75% ALCOHOL HAND SANITIZER

75% ALCOHOL HAND SANITIZER by

Drug Labeling and Warnings

75% ALCOHOL HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by FUYUE BIO-TECHNOLOGY CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

75% ALCOHOL HAND SANITIZER- ethyl alcohol liquid 
FUYUE BIO-TECHNOLOGY CO., LTD.

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75% ALCOHOL HAND SANITIZER

Drug Facts

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

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

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

Stop use and ask a doctor if irritation or redness occurs.

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

Directions

Place enough product in hand palm and rub it until dry.

Inactive Ingredients

Water, Hydroxyethylcellulose, Panthenol, Fragrance

Made In Taiwan

Manufactured by FU YUE Bio-Technology Co., LTD

Packaging

75% ALCOHOL HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81323-621
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
PANTHENOL (UNII: WV9CM0O67Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81323-621-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
2	NDC: 81323-621-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
3	NDC: 81323-621-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
4	NDC: 81323-621-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
5	NDC: 81323-621-05	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
6	NDC: 81323-621-06	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
7	NDC: 81323-621-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
8	NDC: 81323-621-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
9	NDC: 81323-621-09	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024
10	NDC: 81323-621-10	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/13/2021	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/13/2021	12/31/2024

Labeler - FUYUE BIO-TECHNOLOGY CO., LTD. (656370626)

Establishment
Name	Address	ID/FEI	Business Operations
FUYUE BIO-TECHNOLOGY CO., LTD.		656370626	manufacture(81323-621)

Revised: 2/2025

Document Id: 1e78ac33-a754-4386-95f2-6b56381266ee

34390-5

Set id: 0d2c8673-c490-4878-808c-7e6c348c4197

Version: 2

Effective Time: 20250206