Hand Sanitizer by Guangzhou caolvxiang Biotechnology Co.,Ltd HAND SANITIZER gel

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Guangzhou caolvxiang Biotechnology Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria that poterntially can cuase disease. For use when soap and water are not available.

Warnings

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

Do not use

in children less than 2 rnonths of age
on open skin worunds

WHEN USING SECTION

keep out of eyes.ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs.
These rnay be signs of a serious condition.

Keep out of reach of children

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

Directions

Place enough product on hands to cover all surfaces, Rub hands together until dry.
Supervise clhildren under 6 years of age when using this product to avoid swallowing.

Other information

Store between 15-30°C(59-86F)
Avoid freezing and excessive heat above 40°C(104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78414-002
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
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78414-002-06	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
2	NDC: 78414-002-07	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
3	NDC: 78414-002-08	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
4	NDC: 78414-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
5	NDC: 78414-002-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
6	NDC: 78414-002-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
7	NDC: 78414-002-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020
8	NDC: 78414-002-05	350 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/28/2020

Labeler - Guangzhou caolvxiang Biotechnology Co.,Ltd (547949400)

Registrant - Guangzhou caolvxiang Biotechnology Co.,Ltd (547949400)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou caolvxiang Biotechnology Co.,Ltd		547949400	manufacture(78414-002)