MERCI HANDY RAINBOWTIFUL HAND SANITIZER- alcohol 
MERCI HANDY CORPORATION

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.

----------

Merci Handy Rainbowtiful Hand Sanitizer

Drug Facts

Active ingredient

Alcohol 67%

Purpose

Antiseptic

Use

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

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

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

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

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

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

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

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

Kit

Package Labeling: MYSTIC FRUITS

Label7

Package Labeling: NAMASTE

Box

Package Labeling: COCO RICO

RICO

Package Labeling:INTO THE WILD

Label2

Package Labeling:HELLO SUNSHINE

Label3

Package Labeling:DOLCE VITA

Label4

Package Labeling:Cherie Cherry

Label5

Package Labeling:FLOWER POWER

Label6

MERCI HANDY RAINBOWTIFUL HAND SANITIZER 
alcohol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72866-013
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-013-011 in 1 KIT01/01/202106/30/2025
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 30 mL
Part 21 BOTTLE 30 mL
Part 31 BOTTLE 30 mL
Part 41 BOTTLE 30 mL
Part 51 BOTTLE 30 mL
Part 61 BOTTLE 30 mL
Part 71 BOTTLE 30 mL
Part 81 BOTTLE 30 mL
Part 1 of 8
HAND SANITIZER, MYSTIC FRUITS 
alcohol gel
Product Information
Item Code (Source)NDC:72866-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-005-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 2 of 8
HAND SANITIZER, NAMASTE 
alcohol gel
Product Information
Item Code (Source)NDC:72866-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-002-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 3 of 8
HAND SANITIZER, COCO RICO 
alcohol gel
Product Information
Item Code (Source)NDC:72866-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-006-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 4 of 8
HAND SANITIZER, INTO THE WILD 
alcohol gel
Product Information
Item Code (Source)NDC:72866-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-008-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 5 of 8
HAND SANITIZER, HELLO SUNSHINE 
alcohol gel
Product Information
Item Code (Source)NDC:72866-000
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
.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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-000-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 6 of 8
HAND SANITIZER, DOLCE VITA 
alcohol gel
Product Information
Item Code (Source)NDC:72866-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-007-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 7 of 8
HAND SANITIZER CHERIE CHERRY 
alcohol gel
Product Information
Item Code (Source)NDC:72866-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.67 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-010-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Part 8 of 8
HAND SANITIZER, FLOWER POWER 
alcohol gel
Product Information
Item Code (Source)NDC:72866-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL670 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-001-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/01/202106/30/2025
Labeler - MERCI HANDY CORPORATION (118006306)

Revised: 11/2022
Document Id: ee9fa14d-4793-1232-e053-2995a90aed3c
Set id: b4644afc-498d-5e01-e053-2995a90a3485
Version: 2
Effective Time: 20221129
 
MERCI HANDY CORPORATION