HAND SANITIZER AM/PM HAND- ethyl alcohol gel

Hand Sanitizer AM/PM Hand by

Drug Labeling and Warnings

Hand Sanitizer AM/PM Hand 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

Dist. by

GlowBiotics

Phoenix, AZ 85034

Made in USA 877.423.1314

2 Scarth Road Barnes London SW13 OND UK

www.glowbiotics.com

INGREDIENTS AND APPEARANCE

HAND SANITIZER AM/PM HAND 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4186
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: 62742-4186-1	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/21/2020

Labeler - Allure Labs Inc (926831603)