DC WONDER WOMAN MOISTURIZING HAND CLEANSER WITH ALCOHOL JASMINE AND INDIGO- alcohol gel 
MAD Beauty USA 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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DC Wonder Woman Moisturizing Hand Cleanser with Alcohol Jasmine & Indigo

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:

Label6

DC WONDER WOMAN MOISTURIZING HAND CLEANSER WITH ALCOHOL JASMINE AND INDIGO 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78789-054
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.69 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78789-054-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/202012/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/15/202012/31/2024
Labeler - MAD Beauty USA LLC (117508758)

Revised: 12/2021
Document Id: d2a96bf7-b8fc-65bd-e053-2995a90af869
Set id: b3d8eed8-458f-ee2d-e053-2a95a90a9efb
Version: 2
Effective Time: 20211208
 
MAD Beauty USA LLC