Minnie Mouse Cherry Scented Hand Sanitizer by Taste Beauty LLC Drug Facts

Minnie Mouse Cherry Scented Hand Sanitizer by

Drug Labeling and Warnings

Minnie Mouse Cherry Scented Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Taste Beauty LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MINNIE MOUSE CHERRY SCENTED HAND SANITIZER- alcohol gel 
Taste Beauty LLC

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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Drug Facts

Active ingredient

Alcohol Denat. 62% v/v

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only.

Flammable. Keep away from fire and flames.

Do not use

  • In children less than 2 months of age
  • On open skin wounds

When using this product

  • Keep out of eyes, ears and mouth.
  • In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

  • Irritation and redness develop.

These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C(104°F)

Inactive ingredients

Water/Aqua/Eau, Fragrance/Parfum, PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate, FD&C Red No. 40 (Cl 16035), D&C Red No.33 (Cl 17200)

Principal Display Panel – 30 mL Bottle Label

HAND SANITIZER
CHERRY SCENTED

1 FL OZ/30 mL

Figure
MINNIE MOUSE CHERRY SCENTED HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 74825-9023
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Polyethylene Glycol 2000 (UNII: HAF0412YIT)  
Hydrogenated Castor Oil (UNII: ZF94AP8MEY)  
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked) (UNII: 59TL3WG5CO)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Denatonium Benzoate (UNII: 4YK5Z54AT2)  
FD&C Red No. 40 (UNII: WZB9127XOA)  
D&C Red No. 33 (UNII: 9DBA0SBB0L)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 74825-9023-130 mL in 1 BOTTLE; Type 0: Not a Combination Product07/31/202012/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/31/202012/31/2023
Labeler - Taste Beauty LLC (080073601)

Revised: 1/2022
 

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