FOAM HAND SANITIZER liquid

Foam Hand Sanitizer by

Drug Labeling and Warnings

Foam Hand Sanitizer 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

Sodium chloride 1.5%

Purpose

Antiseptic

Uses

Apply proper amount to palm, massage gently until foamy, then rinse with water.

Warnings

This product is for external use only.

When using this product In case of contact with eyes, rinse immediately with plenty of water.

Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame

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

DO NOT USE

/

WHEN USING

When using this product In case of contact with eyes, rinse immediately with plenty of water.

Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame

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

STOP USE

Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame

KEEP OUT OF REACH OF CHILDREN

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

Directions

Scope of application: Household and personal cleaning.
Main Effect Effective inhibition of microorganisms category intestinal bacteria, pyogenic coccus.

Other information

Keep tightly closed. Store between 32°F and 109°F

Inactive ingredients

Citric acid, Cocoamidopropyl betaine, Coconut oil amide DEA, Disodium EDTA, DMDM hydantoin, Essence, Sodium lauryl alcohol polyether sulfate, Water

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

FOAM HAND SANITIZER 
foam hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75132-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	1.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO DIETHANOLAMIDE (UNII: 92005F972D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
DMDM HYDANTOIN (UNII: BYR0546TOW)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
METHYL BENZOATE (UNII: 6618K1VJ9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75132-012-03	950 mL in 1 BAG; Type 0: Not a Combination Product	04/12/2020
2	NDC: 75132-012-01	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2020
3	NDC: 75132-012-02	950 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 final	part349	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(75132-012)