GOLDEN GROOMING COMPANY HAND SANITIZER- ethyl alcohol gel

GOLDEN GROOMING COMPANY HAND SANITIZER by

Drug Labeling and Warnings

GOLDEN GROOMING COMPANY HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Square M Llc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient(s)

ethyl alcohol 70% v/v

Purpose

Antiseptic

INDICATIONS & USAGE

Use(s) Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warning

For external use only. Flammable. Keep away from heat or flame

Do not use:

■ in children less than 2 months of age

■ on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Directions

■ Place enough product on hands to cover all surfaces. Rub hands together until dry.

■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

■ Store between 15-30C (59-86F)

■ Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

water, glycerin, PEG-6 (AND) AMP-acrylates/vinyl isodecanoate crosspolymer, fragrance, aloe barbadensis (aloe vera) leaf juice, tocopheryl acetate (vitamin E acetate)

SPL UNCLASSIFIED SECTION

70% ETHYL ALCOHOL GEL

WITH MOISTURIZING ALOE & VITAMIN E

Squeeze a bead of gel into your palm large enough to cover your whole hands, including between your fingers and around your thumbs. People are always forgetting those areas.

Made in USA

Visit us at: goldengroomingco.com

Manufactured for Golden Grooming by:

Square M LLC

Sterling Heights, MI 48314

Packaging

INGREDIENTS AND APPEARANCE

GOLDEN GROOMING COMPANY HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73834-202
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
VINYL NEODECANOATE (UNII: 9NDY01YYPT)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73834-202-16	474 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/06/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/06/2020

Labeler - Square M Llc (117467455)

Establishment
Name	Address	ID/FEI	Business Operations
Square M Llc		117467455	manufacture(73834-202)