FA Hand Sanitizer by FA Inc.

FA Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

FA HAND SANITIZER- ethyl alcohol gel 
HLB CO.,LTD_Healthcare

----------

ACTIVE INGREDIENT

Ethyl Alcohol 70% w/w

INACTIVE INGREDIENTS

Carbomer, Fragrance, Glycerin, Triethanolamine, Water

PURPOSE

Antiseptic

WARNINGS

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

--------------------------------------------------------------------------------------------------------
When using 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 Poison Control Center right away.

Uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

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 below 86℉(Between 1~30℃)

■ May discolor certain fabrics or surfaces

FA HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74932-320
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)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74932-320-02	50 in 1 CARTON	06/01/2020	12/30/2022
1	NDC: 74932-320-01	2 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 74932-320-03	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/30/2022
3	NDC: 74932-320-04	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/01/2020	12/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/01/2020	12/30/2022

Labeler - HLB CO.,LTD_Healthcare (987587913)

Registrant - HLB CO.,LTD_Healthcare (987587913)

Establishment
Name	Address	ID/FEI	Business Operations
HLB CO.,LTD_Healthcare		987587913	manufacture(74932-320)

Revised: 7/2024

Document Id: 1ceec9aa-8d4e-f87e-e063-6294a90a096d

34390-5

Set id: 11876a16-8c6f-4b51-827c-033dff81edab

Version: 6

Effective Time: 20240711