75% ALCOHOL DISINFECTANT- 75% alcohol disinfectant liquid
Guangdong Kemei Pharmaceutical Technology Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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75% Alcohol Disinfectant

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.

Do not take it orally.

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

Keep out of reach of children and Allergies are disabled.

Directions

On cleaning and disinfecting the surface of hands, skin

and general objects Using to wipe, apply or spray the

disinfected part 1-2 times, the action time is 1-3

minutes.

Other information

Keep away from fire
Place in a cool and dry place

Inactive ingredients

Package Label - Principal Display Panel

236 1000 3785 300 100 500

75% ALCOHOL DISINFECTANT
75% alcohol disinfectant liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75132-002
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:75132-002-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
2	NDC:75132-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
3	NDC:75132-002-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
4	NDC:75132-002-04	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
5	NDC:75132-002-05	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
6	NDC:75132-002-06	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
7	NDC:75132-002-07	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
8	NDC:75132-002-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
9	NDC:75132-002-09	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
10	NDC:75132-002-10	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020

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

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

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

Name	Address	ID/FEI	Business Operations
Establishment
Guangdong Kemei Pharmaceutical Technology Co., Ltd.		554528507	manufacture(75132-002)