Warner Friends Sanitizer Clip and Clean, HOW U DOIN Coconut

Warner Friends Sanitizer Clip and Clean, HOW U DOIN Coconut by

Drug Labeling and Warnings

Warner Friends Sanitizer Clip and Clean, HOW U DOIN Coconut by is a Otc medication manufactured, distributed, or labeled by Mad Beauty USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNER FRIENDS SANITIZER CLIP AND CLEAN, HOW U DOIN COCONUT- 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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Warner Friends Sanitizer Clip and Clean, HOW U DOIN Coconut

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

• Place pea sized drop onto hands.
• Supervise children under 6 years of age when using this produt 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), Pentylene Glycol, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Butylene Glycol, Fragrance(Parfum), Sodium Hydroxide, Aloe Barbadensis (Aloe Vera)Leaf Extract, CI 42090(FD&C Blue1).

Questions or Comments

MAD BEAUTY USA LLC

1030 SALEM ROAD

UNION NJ 07083 

TEL (844) 995 1701

Package Labeling:

WARNER FRIENDS SANITIZER CLIP AND CLEAN, HOW U DOIN COCONUT 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78789-042
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)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78789-042-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/09/2020	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/09/2020	12/31/2024

Labeler - Mad Beauty USA LLC (117508758)

Revised: 12/2021

Document Id: d2bd5cac-18d8-f321-e053-2a95a90a24ab

34390-5

Set id: ae6db3ca-741d-1ddf-e053-2995a90a24c7

Version: 2

Effective Time: 20211209