DISNEY MARIE MOISTURIZING HAND SANITIZER, STRAWBERRY- alcohol gel

Disney Marie Moisturizing Hand Sanitizer, STRAWBERRY by

Drug Labeling and Warnings

Disney Marie Moisturizing Hand Sanitizer, STRAWBERRY by is a Otc medication manufactured, distributed, or labeled by Mad Beauty USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Active Ingredient

Ethylalcohol 69%

Purpose

Antimicrobial

Uses

Reduce bacteria on hands.

Warnings

Flammable. Keep away from source of Ignition or flame.

For external use only.

Do not use

on open skin wounds

When using this product

keep out of eyes.

Stop use and ask a doctor

if irritation or redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a doctor immediately.

Directions

Spray into hands. Rub until absorbed.

Supervise children under 6 years of age when using this produt to avoid swallowing.

Inactive Ingredients

Water(Aqua)/Eau, pentylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Fragrance(parfum), Sodium Hydroxide, Aloe Barbadensis (Aloe Vera)Leaf Extract.

Other Information

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

Questions or Comments

MAD BEAUTY USA LLC

1030 SALEM ROAD

UNION NJ 07083 MARYLAND

TEL (844) 995 1701

Package Labeling:

INGREDIENTS AND APPEARANCE

DISNEY MARIE MOISTURIZING HAND SANITIZER, STRAWBERRY 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78789-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.69 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78789-024-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/20/2020	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/20/2020	12/31/2024

Labeler - Mad Beauty USA LLC (117508758)