ALCOHOL-BASED DISINFECTANT HAND SANITIZER gel

ALCOHOL-BASED DISINFECTANT HAND SANITIZER by

Drug Labeling and Warnings

ALCOHOL-BASED DISINFECTANT HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Foshan Lang-Yeon Trade Limited Company, GUIZHOU XINZIHONG PHARMACEUTIC ADJUVANT CO.LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75% v/v. Purpose: Antimicrobial

Purpose

Purpose: Antimicrobial , Hand Sanitizer

Use

Pour a suitable amount of gel onto the palm of your hand and rub hands together thoroughly. Gel will evaporate. No need to rinse or dry hands after use

Warnings

Keep out of reach of children This product is highly flammable Keep away from open flame or fire Avoid contact with eyes and mucous membranes Harmful if swallowed

Do not use

/

WHEN USING

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STOP USE

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KEEP OUT OF REACH OF CHILDREN

Directions

This product has a strong inhibitoryffect on various bacteria and virusesincluding Staphylococcus Aureus,

Pseudomonas Aeruginosa, CandidaAlbcans and Escherichia Coli

Other information

Keep in a cool, dry and well ventilated area away from direct sunlight

Inactive ingredients

Water, Glycerin, Carbomer,Triethanolamine, Lavender Essence

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ALCOHOL-BASED DISINFECTANT HAND SANITIZER 
alcohol-based disinfectant hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79606-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
LAVENDER OIL (UNII: ZBP1YXW0H8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79606-002-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
2	NDC: 79606-002-03	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
3	NDC: 79606-002-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
4	NDC: 79606-002-02	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
5	NDC: 79606-002-05	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
6	NDC: 79606-002-06	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
7	NDC: 79606-002-07	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
8	NDC: 79606-002-08	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
9	NDC: 79606-002-09	3000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
10	NDC: 79606-002-10	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020
11	NDC: 79606-002-11	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/10/2020

Labeler - Foshan Lang-Yeon Trade Limited Company (554537424)

Establishment
Name	Address	ID/FEI	Business Operations
GUIZHOU XINZIHONG PHARMACEUTIC ADJUVANT CO.LTD		540725476	manufacture(79606-002)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Lang-Yeon Trade Limited Company		554537424	label(79606-002)