HAND SANITIZER- hand sanitizer spray spray

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer 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

Use: Hand sanitizer to help, reduce bacteria on skin

Warnings

Warnings. Flammable. Keep away from fire or flame For extend use or 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 a doctor if imitation or rash appears and lasts. Keep out of reach of children. I swallowed, get medical help or contact a Poison Control Center immediately

DO NOT USE

When using this product do not use in or near the eyes

WHEN USING THIS PRODUCT

When using this product do not use in or near the eyes.

STOP USE

stop use and ask a doctor if imitation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Directions

Directions: Put enough product n your palm to cover hands and rub hands together brady until dry

Children 6 years of age should be supervised when using

Other information

Other information: Store at room temperature

Keep container tightly closed in a dry and well-ventilated place

Avoid storage under direct sunlight

Keep out of reach of children

Inactive ingredients

Inactive ingredients: Water (Aqua), Isopropyl Alcohol , Aloe Barbadensis Leaf Juice,

Caprylyl Glycol, Glycerin, Isopropyl Miristate, Acrylates/C10-30 Alky Acrylate Cross polymer,

Aminomethyl Propanol, Fragrance(Parfum)

Package Label - Principal Display Panel

74881-005-01 150ml

74881-005-02 150ml

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
hand sanitizer spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74881-005
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
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
1-AMINOBUTAN-2-OL (UNII: 19453GN3YQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74881-005-01	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/23/2020
2	NDC: 74881-005-02	150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/23/2020

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(74881-005)