DC WONDER WOMAN MOISTURIZING HAND CLEANSER WITH ALCOHOL JASMINE AND INDIGO- alcohol gel

DC Wonder Woman Moisturizing Hand Cleanser with Alcohol Jasmine and Indigo by

Drug Labeling and Warnings

DC Wonder Woman Moisturizing Hand Cleanser with Alcohol Jasmine and Indigo 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

Reduces bacteria on hands.

Warnings

Flammable. Keep away from source of Ignition or flame.

For external use only.

Do not use 

on open skin wound.

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

Place pea sized drop onto hands. 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), Pentylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Fragrance(Parfum), Sodium Hydroxide, Aloe Barbadensis (Aloe Vera) Leaf Extract.

Questions or Comments

MAD BEAUTY USA LLC 1030 SALEM ROAD UNION NJ 07083 TEL (844) 995 1701

Package Labeling:

INGREDIENTS AND APPEARANCE

DC WONDER WOMAN MOISTURIZING HAND CLEANSER WITH ALCOHOL JASMINE AND INDIGO 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78789-054
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)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
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: 78789-054-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2020	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/15/2020	12/31/2024

Labeler - MAD Beauty USA LLC (117508758)