DailyMed - MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET- alcohol kit

NDC Code(s): 72866-017-01, 72866-018-01, 72866-019-01, 72866-020-01, view more
72866-021-01, 72866-022-01, 72866-023-01, 72866-024-01, 72866-025-01, 72866-026-01, 72866-027-01, 72866-028-01, 72866-029-01
Packager: MERCI HANDY CORPORATION

Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated January 23, 2024

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Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, FD&C Red No.4, D&C Red No.33, D&C Red No.30
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Limonene, Citral, FD&C Yellow No. 5, Chromium Oxide Greens, FD&C Blue No.1.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Linalool, Alpha-Isomethyl Ionone, Citronellol, Geraniol, Limonene, Ferric Ferrocyanide, FD&C Blue No.1
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Linalool, Hexyl Cinnamal, Geraniol, Limonene, D&C Red No.33, D&C Red No.30
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Synthetic Fluorphlogopite, Coumarin, Limonene, Alpha-Isomethyl Ionone, Cinnamyl Alcohol, Isoeugenol, Titanium Dioxide, FD&C Yellow No. 5, Iron Oxides, FD&C Red No. 4.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Citronellol, Linalool, Limonene, Yellow No. 5, FD&C Red No. 4, Iron Oxides.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Linalool, Hexyl Cinnamal, FD&C Blue No. 1, Ferric Ferrocyanide.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.
Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use anKeep out of reach of childrend ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Eugenol, Coumarin, Isoeugenol, Limonene, FD&C Red No. 4, D&C Red No. 33, D&C Red No. 30.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Hexyl Cinnamal, Citronellol, Linalool, Alpha-Isomethyl Ionone, Limonene, Ferrocyanide, D&C Red No. 33, FD&C Blue No. 1.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Benzyl Salicylate, Linalool, Geraniol, Citronellol, Limonene, FD&C Yellow No. 5, FD&C Red No. 4, Iron Oxides.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Benzyl Benzoate, Limonene, Hexyl Cinnamal, FD&C Blue No. 1, D&C Red No. 33, Ferric Ferrocyanide.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67% (v/v)

Purpose

Antiseptic
Use
- for handwashing to decrease bacteria on the skin
Warnings
For external use only.

Flammable keep away from fire or flame.

Do not use

in the eyes. In the case of contact, flush eyes with water.
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away
Directions

wet hands thoroughly with product and allow to dry without wiping
Other information

store at a temperature below 110° F (43° C)
Inactive Ingredients

Aqua (Water), Parfum (Fragrance), Aloe Barbadensis Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Zea Mays (Corn) Starch, Denatonium Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Linalool, Hexyl Cinnamal, Benzyl Salicylate, Alpha-Isomethyl Ionone, FD&C Yellow No. 5, Chromium Oxide Greens, FD&C Blue No. 1.
QUESTIONS OR COMMENTS?

(646)-358-3432
Package Labeling:72866-017-01
Package Labeling:72866-018-01
Package Labeling:72866-019-01
Package Labeling:72866-020-01
Package Labeling:72866-021-01
Package Labeling:72866-022-01
Package Labeling:72866-023-01
Package Labeling:72866-024-01
Package Labeling:72866-025-01
Package Labeling:72866-026-01
Package Labeling:72866-027-01
Package Labeling:72866-028-01
Package Labeling:72866-029-01

INGREDIENTS AND APPEARANCE

MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET
alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72866-017

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-017-01	1 in 1 KIT	05/01/2021	12/31/2026

Part #	Package Quantity	Total Product Quantity
Quantity of Parts
Part 1	1 BOTTLE	30 mL
Part 2	1 BOTTLE	30 mL
Part 3	1 BOTTLE	30 mL
Part 4	1 BOTTLE	30 mL
Part 5	1 BOTTLE	30 mL
Part 6	1 BOTTLE	30 mL
Part 7	1 BOTTLE	30 mL
Part 8	1 BOTTLE	30 mL
Part 9	1 BOTTLE	30 mL
Part 10	1 BOTTLE	30 mL
Part 11	1 BOTTLE	30 mL
Part 12	1 BOTTLE	30 mL

Part 1 of 12

MERCI HANDY SANCTUARY HAND SANITIZER ARIES
alcohol gel

Product Information
Item Code (Source)	NDC:72866-018
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C RED NO. 30 (UNII: 2S42T2808B)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-018-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 2 of 12

MERCI HANDY SANCTUARY HAND SANITIZER TAURUS
alcohol gel

Product Information
Item Code (Source)	NDC:72866-019
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
CITRAL (UNII: T7EU0O9VPP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
CHROMIC OXIDE (UNII: X5Z09SU859)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-019-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 3 of 12

MERCI HANDY SANCTUARY HAND SANITIZER GEMINI
alcohol gel

Product Information
Item Code (Source)	NDC:72866-020
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
GERANIOL (UNII: L837108USY)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FERRIC FERROCYANIDE (UNII: TLE294X33A)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-020-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 4 of 12

MERCI HANDY SANCTUARY HAND SANITIZER CANCER
alcohol gel

Product Information
Item Code (Source)	NDC:72866-021
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
GERANIOL (UNII: L837108USY)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C RED NO. 30 (UNII: 2S42T2808B)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-021-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 5 of 12

MERCI HANDY SANCTUARY HAND SANITIZER LEO
alcohol gel

Product Information
Item Code (Source)	NDC:72866-022
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
COUMARIN (UNII: A4VZ22K1WT)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
CINNAMYL ALCOHOL (UNII: SS8YOP444F)
ISOEUGENOL (UNII: 5M0MWY797U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-022-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 6 of 12

MERCI HANDY SANCTUARY HAND SANITIZER VIRGO
alcohol gel

Product Information
Item Code (Source)	NDC:72866-023
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FERRIC OXIDE RED (UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-023-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 7 of 12

MERCI HANDY SANCTUARY HAND SANITIZER LIBRA
alcohol gel

Product Information
Item Code (Source)	NDC:72866-024
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FERRIC FERROCYANIDE (UNII: TLE294X33A)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-024-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 8 of 12

MERCI HANDY SANCTUARY HAND SANITIZER SCORPIO
alcohol gel

Product Information
Item Code (Source)	NDC:72866-025
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EUGENOL (UNII: 3T8H1794QW)
COUMARIN (UNII: A4VZ22K1WT)
ISOEUGENOL (UNII: 5M0MWY797U)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C RED NO. 30 (UNII: 2S42T2808B)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-025-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 9 of 12

MERCI HANDY SANCTUARY HAND SANITIZER SAGITTARIUS
alcohol gel

Product Information
Item Code (Source)	NDC:72866-026
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FERROCYANIDE ION (UNII: FLX0VIC39Y)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-026-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 10 of 12

MERCI HANDY SANCTUARY HAND SANITIZER CAPRICORN
alcohol gel

Product Information
Item Code (Source)	NDC:72866-027
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
GERANIOL (UNII: L837108USY)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FERRIC OXIDE RED (UNII: 1K09F3G675)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-027-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 11 of 12

MERCI HANDY SANCTUARY HAND SANITIZER AQUARIUS
alcohol gel

Product Information
Item Code (Source)	NDC:72866-028
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BENZYL BENZOATE (UNII: N863NB338G)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FERRIC FERROCYANIDE (UNII: TLE294X33A)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-028-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Part 12 of 12

MERCI HANDY SANCTUARY HAND SANITIZER PISCES
alcohol gel

Product Information
Item Code (Source)	NDC:72866-029
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	67 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SUCROSE (UNII: C151H8M554)
CORN (UNII: 0N8672707O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
CHROMIC OXIDE (UNII: X5Z09SU859)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-029-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/01/2021	12/31/2026

Labeler - MERCI HANDY CORPORATION (118006306)

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Published Date (What is this?)	Version	Files
Jan 24, 2024	3 (current)	download
Dec 2, 2022	2	download
May 3, 2021	1	download

	RxCUI	RxNorm NAME	RxTTY
1	1039708	ethanol 67 % Topical Gel	PSN
2	1039708	ethanol 0.67 ML/ML Topical Gel	SCD
3	1039708	ethanol 67 % Topical Gel	SY

	NDC
1	72866-017-01
2	72866-018-01
3	72866-019-01
4	72866-020-01
5	72866-021-01
6	72866-022-01
7	72866-023-01
8	72866-024-01
9	72866-025-01
10	72866-026-01
11	72866-027-01
12	72866-028-01
13	72866-029-01

Label: MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET- alcohol kit

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Keep out of reach of children

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Keep out of reach of children

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Keep out of reach of children

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Keep out of reach of children

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Stop use anKeep out of reach of childrend ask a doctor if

Keep out of reach of children

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Stop use and ask a doctor if

Keep out of reach of children

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Stop use and ask a doctor if

Keep out of reach of children

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Do not use

Stop use and ask a doctor if

Keep out of reach of children

Purpose

Do not use

Stop use and ask a doctor if

Keep out of reach of children

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MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET- alcohol kit

Number of versions: 3

MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET- alcohol kit

MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET- alcohol kit

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MERCI HANDY SANCTUARY HAND SANITIZER ZODIAC SET- alcohol kit

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.