FA HAND SANITIZER GEL 70% (ETHANOL)- hand sanitizer gel

FA Hand Sanitizer Gel 70% (Ethanol) by

Drug Labeling and Warnings

FA Hand Sanitizer Gel 70% (Ethanol) by is a Otc medication manufactured, distributed, or labeled by HLB CO.,LTD_Healthcare. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria on the skin.

Recommended for repeated use.

Warnings

For external use only - hands

Flammable, Keep awa from fire or flame

When useing this product

-do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

-avoid contact with broken skin.

-do not inhale or ingest.

Stop use and ask a doctor if

irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poision Control Center right away.

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.

Not recommended for infants.

Other information

Store below 86 oF (Between 1 oC-30 oC).

May discolor certain fabrics or surfaces.

Inactive Ingredients

Carbormer, Fragrance, Glycerin, Triethanolamine, Water.

Package Label

INGREDIENTS AND APPEARANCE

FA HAND SANITIZER GEL 70% (ETHANOL) 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74932-100
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
GLYCERIN (UNII: PDC6A3C0OX)

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74932-100-01	1 in 1 BOX	04/10/2020
1		57 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/10/2020

Labeler - FA Inc. (557816103)

Registrant - FA Inc. (557816103)

Establishment
Name	Address	ID/FEI	Business Operations
FA Inc.		557816103	manufacture(74932-100)