DISINFECTION HAND SANITIZER GEL gel

DISINFECTION HAND SANITIZER GEl by

Drug Labeling and Warnings

DISINFECTION HAND SANITIZER GEl by is a Otc medication manufactured, distributed, or labeled by Huizhou Baozi Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antimicrobial

Uses

Hand reduce bacteria on 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 and ask doctor if irritation or rash appears and lasts.Keep out of reach for children. if swallowed,get medical help or contact a With Vitamin E& Poison Control Center right away.

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.

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

Other information

Store below 106°F(41°C)

May discolor certain fabrics or surfaces

Inactive ingredients

Water,carbomer,triethanolamine

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

DISINFECTION HAND SANITIZER GEL 
disinfection hand sanitizer gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74881-001
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74881-001-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
2	NDC: 74881-001-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
3	NDC: 74881-001-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Huizhou Baozi Biotechnology Co., Ltd. (419304583)

Registrant - Huizhou Baozi Biotechnology Co., Ltd. (419304583)

Establishment
Name	Address	ID/FEI	Business Operations
Huizhou Baozi Biotechnology Co., Ltd.		419304583	manufacture(74881-001)