WASH-FREE HAND SANITIZER GEL 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

Uses Hand Sanitizer to help reduce bacteria on skin

Warnings

This product is sterilized for external use.
Do not take it orally.
Keep out of reach of children and Allergies are disabled.
When using, do not contact with eyes, rinse with water immediately and consult a doctor in case of contract.

DO NOT USE

Do not take it orally.

WHEN USING

When using, do not contact with eyes, rinse with water immediately and consult a doctor in case of contract.

STOP USE

/

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and Allergies are disabled.

Directions

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

completely dry.

Other information

Keep away from fire
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 
wash-free hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75132-011
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)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75132-011-01	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
2	NDC: 75132-011-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
3	NDC: 75132-011-03	3785 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(75132-011)