HAND SANITIZER, GLITTER FEVER- alcohol gel 
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.

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Hand Sanitizer, Glitter Fever

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, Denatonium Benzoate, Tocopheryl Acetate,
Maltodextrin, Hydroxypropyl Methylcellulose, Potassium Sorbate, Sodium Benzoate, 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

Package Labeling:

Label4

HAND SANITIZER, GLITTER FEVER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72866-009
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)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
COUMARIN (UNII: A4VZ22K1WT)  
LIMONENE, (+)- (UNII: GFD7C86Q1W)  
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72866-009-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product03/10/202006/30/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E03/01/202006/30/2025
Labeler - Merci Handy Corporation (118006306)

Revised: 11/2022
Document Id: eea07c75-2fed-2cae-e053-2a95a90a08b0
Set id: 957c51c2-ab0b-4785-bba7-6f4f83e38dae
Version: 4
Effective Time: 20221129
 
Merci Handy Corporation