VISIBLY CLEAN HAND SANITIZER- alcohol gel

Visibly Clean Hand Sanitizer by

Drug Labeling and Warnings

Visibly Clean Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Brands International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Ethyl Alcohol 70%w/w.

Purpose: Antiseptic

Purpose

Antiseptic

Safety Instructions

Flammable, Keep away from fire and flame

Ask Doctor

Stop Use and Ask a doctor if irritation or redness develops

KEEP OUT OF REACH OF CHILDREN

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

Other Information

Store below 110°F (43°C)
May discolor certain fabrics or surfaces.

Inactive Ingredients

water, isopropyl alcohol, glycerin, carbomer, aminomethyl propanol, fragrance, propylene glycol, isopropyl myristate, propylene glycol, Aloe, Tocopheryl Acetate. Please review Label for further details

Directions

• Place enough product in your palm to thoroughly cover your hands
• Rub hands together briskly until dry
• Children under 6 years of age should be supervised when using this product.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Uses

• helps reduce bacteria on the skin that could cause disease
• Recommended for repeated use

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VISIBLY CLEAN HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-335
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-335-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/02/2020
2	NDC: 50157-335-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/02/2020

Labeler - Brands International (243748238)