DailyMed - MERCI HANDY RAINBOWTIFUL HAND SANITIZER- alcohol kit

NDC Code(s): 72866-000-30, 72866-001-30, 72866-002-30, 72866-005-30, view more
72866-006-30, 72866-007-30, 72866-008-30, 72866-010-30, 72866-013-01
Packager: MERCI HANDY CORPORATION

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None
Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 29, 2022

If you are a consumer or patient please visit this version.

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Drug Facts
Active ingredient

Alcohol 67%

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 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

Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium 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%

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 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

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

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67%

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 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

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

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67%

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 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

Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, 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%

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 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.
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

Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, Amyl Cinnamal, Hexyl Cinnamal, Benzyl Salicylate, Alpha-Isomethyl Ionone, Amycinnamyl Alcohol, FD&C Yellow No.5, FD&C Red No. 4, Iron Oxides.
QUESTIONS OR COMMENTS?

(646)-358-3432
Drug Facts
Active ingredient

Alcohol 67%

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 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

Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, 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%

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 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

Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch, 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%

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 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

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

(646)-358-3432
Package Labeling:Kit
Package Labeling: MYSTIC FRUITS
Package Labeling: NAMASTE
Package Labeling: COCO RICO
Package Labeling:INTO THE WILD
Package Labeling:HELLO SUNSHINE
Package Labeling:DOLCE VITA
Package Labeling:Cherie Cherry
Package Labeling:FLOWER POWER

INGREDIENTS AND APPEARANCE

MERCI HANDY RAINBOWTIFUL HAND SANITIZER
alcohol kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72866-013

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-013-01	1 in 1 KIT	01/01/2021	06/30/2025

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 1 of 8

HAND SANITIZER, MYSTIC FRUITS
alcohol gel

Product Information
Item Code (Source)	NDC:72866-005
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
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:72866-005-30	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 not final	part333E	01/01/2021

Part 2 of 8

HAND SANITIZER, NAMASTE
alcohol gel

Product Information
Item Code (Source)	NDC:72866-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FERRIC FERROCYANIDE (UNII: TLE294X33A)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C RED NO. 30 (UNII: 2S42T2808B)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-002-30	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 not final	part333E	01/01/2021

Part 3 of 8

HAND SANITIZER, COCO RICO
alcohol gel

Product Information
Item Code (Source)	NDC:72866-006
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
COUMARIN (UNII: A4VZ22K1WT)
GERANIOL (UNII: L837108USY)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FERRIC FERROCYANIDE (UNII: TLE294X33A)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-006-30	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 not final	part333E	01/01/2021

Part 4 of 8

HAND SANITIZER, INTO THE WILD
alcohol gel

Product Information
Item Code (Source)	NDC:72866-008
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 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)
.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:72866-008-30	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 not final	part333E	01/01/2021

Part 5 of 8

HAND SANITIZER, HELLO SUNSHINE
alcohol gel

Product Information
Item Code (Source)	NDC:72866-000
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
.ALPHA.-AMYLCINNAMYL ALCOHOL (UNII: DKB52S61GU)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FERRIC OXIDE RED (UNII: 1K09F3G675)
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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-000-30	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 not final	part333E	01/01/2021

Part 6 of 8

HAND SANITIZER, DOLCE VITA
alcohol gel

Product Information
Item Code (Source)	NDC:72866-007
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 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)
.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:72866-007-30	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 not final	part333E	01/01/2021

Part 7 of 8

HAND SANITIZER CHERIE CHERRY
alcohol gel

Product Information
Item Code (Source)	NDC:72866-010
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.67 mL in 1 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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72866-010-30	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 not final	part333E	01/01/2021

Part 8 of 8

HAND SANITIZER, FLOWER POWER
alcohol gel

Product Information
Item Code (Source)	NDC:72866-001
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	670 mg in 1 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)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
.ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
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:72866-001-30	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 not final	part333E	01/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	01/01/2021	06/30/2025

Labeler - MERCI HANDY CORPORATION (118006306)

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Published Date (What is this?)	Version	Files
Nov 30, 2022	2 (current)	download
Jan 6, 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	72866-000-30
2	72866-001-30
3	72866-002-30
4	72866-005-30
5	72866-006-30
6	72866-007-30
7	72866-008-30
8	72866-010-30
9	72866-013-01

Label: MERCI HANDY RAINBOWTIFUL HAND SANITIZER- alcohol kit

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Purpose

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.

Purpose

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.

Purpose

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.

Purpose

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 RAINBOWTIFUL HAND SANITIZER- alcohol kit

Number of versions: 2

MERCI HANDY RAINBOWTIFUL HAND SANITIZER- alcohol kit

MERCI HANDY RAINBOWTIFUL HAND SANITIZER- alcohol kit

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MERCI HANDY RAINBOWTIFUL HAND SANITIZER- alcohol kit

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