WASH-FREE HAND SANITIZER GEL- alcohol gel

Wash-free Hand Sanitizer Gel by

Drug Labeling and Warnings

Wash-free Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Guangdong Kemei Pharmaceutical Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Alcohol 75%

Purpose

Killing microorganism like colibacillus, staphylococcus aureus,candida albicans,

pseudomonas aerugino.

Uses

Hand Sanitizer to help reduce bacteria on skin.

Warnings

This product is sterilized for external use.Do not take it orally.Allergies are

disabled.

When using, do not use in or near eyes.In case of contract,rinse with water immediately.Stop use

and consult a doctor in case of contract.Keep out of reach of children.

DO NOT USE

WHEN USING

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

No water required.Apply 3ml amount to palm,rubbing in hands and fingers until

completely dry.

Other information

Keep away from fire and place in a cool and dry place.

Inactive ingredients

Water, Carbomer, Glycerin, Aminomethyl Propanol

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

WASH-FREE HAND SANITIZER GEL 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75132-001
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
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75132-001-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
2	NDC: 75132-001-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
3	NDC: 75132-001-03	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
4	NDC: 75132-001-04	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
5	NDC: 75132-001-05	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
6	NDC: 75132-001-06	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
7	NDC: 75132-001-07	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
8	NDC: 75132-001-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
9	NDC: 75132-001-09	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
10	NDC: 75132-001-10	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
11	NDC: 75132-001-11	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
12	NDC: 75132-001-12	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
13	NDC: 75132-001-13	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
14	NDC: 75132-001-14	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
15	NDC: 75132-001-15	50000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
16	NDC: 75132-001-16	100000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
17	NDC: 75132-001-17	1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/12/2020

Labeler - Guangdong Kemei Pharmaceutical Technology Co., Ltd. (554528507)

Registrant - Guangdong Kemei Pharmaceutical Technology Co., Ltd. (554528507)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Kemei Pharmaceutical Technology Co., Ltd.		554528507	manufacture(75132-001)