ADVANCED HAND SANITIZER gel

advanced hand sanitizer by

Drug Labeling and Warnings

advanced hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou Fuda Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Ethyl Alcohol 75%(v/v)

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin.

Warnings

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

DO NOT USE

When using this product

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

STOP USE

Stop use and ask a doctor if Irritation or rash appears and/or lasts

Keep out of reach of children

If swallowed get medical help or contact a Poison Control Center right away

Directions

Put enough product in your palm to cover both hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this.

Other information

Store below 110°F(43℃)

May discolor certain fabrics or surfaces

Inactive ingredients

Purified water, Glycerin,Carbomer,Aminomethyl Propanol, Vitamin E

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER 
advanced hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75151-001
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
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75151-001-01	50 mL in 1 AMPULE; Type 0: Not a Combination Product	04/20/2020
2	NDC: 75151-001-02	60 mL in 1 AMPULE; Type 0: Not a Combination Product	04/20/2020
3	NDC: 75151-001-03	100 mL in 1 AMPULE; Type 0: Not a Combination Product	04/20/2020
4	NDC: 75151-001-04	200 mL in 1 AMPULE; Type 0: Not a Combination Product	04/20/2020
5	NDC: 75151-001-05	300 mL in 1 AMPULE; Type 0: Not a Combination Product	04/20/2020
6	NDC: 75151-001-06	500 mL in 1 AMPULE; Type 0: Not a Combination Product	04/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/20/2020

Labeler - Guangzhou Fuda Biotechnology Co., Ltd. (554528964)

Registrant - Guangzhou Fuda Biotechnology Co., Ltd. (554528964)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Fuda Biotechnology Co., Ltd.		554528964	manufacture(75151-001)