HAND SANITIZER- ethyl alcohol gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Allure Labs Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients:

Ethyl Alcohol - 70%

PURPOSE

Purpose: Antimicrobial

INDICATIONS & USAGE

Uses: Helps to reduce bacteria on skin. Recommended for repeated use.

WARNINGS

Warning: For External use only - Hands

Flammable: Keep away from heat and Flame.

WHEN USING

When using this products:

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin.

STOP USE

Stop use and ask a doctor if skin irritation develops. 

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

• If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

• Wet hands throughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

INACTIVE INGREDIENT

Inactive Ingredients: Water (Aqua), Acrylates Copolymer, Glycerin, Sodium Hydroxide.

PRINCIPAL DISPLAY PANEL

MANUFACTURED FOR

ECZEMA HONEY CO BY,

ALLURE LABS,

HAYWARD, CA, 94545

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4187
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4187-1	59 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/23/2020
2	NDC: 62742-4187-2	237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/23/2020

Labeler - Allure Labs Inc (926831603)