LAMWAVE ANTIMICROBIAL HAND SANITIZERS GEL- bacteriostatic gel gel

Lamwave antimicrobial hand sanitizers gel by

Drug Labeling and Warnings

Lamwave antimicrobial hand sanitizers gel by is a Otc medication manufactured, distributed, or labeled by Guangzhou Youmei Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Store below 110°F(43°C). May discolor certain fabrics or surfaces.

INACTIVE INGREDIENT

ethanol

pure water

Carbomer

trimethylpentylenediol / adipic acid / glycerine crosslinked aggregate

triethylamine

PURPOSE

Disinfection
Sterilization

INDICATIONS & USAGE

Put enough product on your palm to cover hands and rub hands together briskly until dry.

ACTIVE INGREDIENT

allantoin

Fermentation products of bacillus

KEEP OUT OF REACH OF CHILDREN

keep out of children

WARNINGS

1.Flammable, Keep away from fire or flame。

2.For external use only When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

3.Stop use and ask a doctor if irritation or rash appears and lasts.

4.Keep out of reach of children. If swallowed，get medical help or contact a poison control center right away.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LAMWAVE ANTIMICROBIAL HAND SANITIZERS GEL 
bacteriostatic gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41878-002
Route of Administration	EXTRACORPOREAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACILLUS AMYLOLIQUEFACIENS (UNII: 1M5Y26M37U) (BACILLUS AMYLOLIQUEFACIENS - UNII:1M5Y26M37U)	BACILLUS AMYLOLIQUEFACIENS	0.05 mg  in 100 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.05 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
TRIMETHYL-1,3-PENTANEDIOL (UNII: WT1X081P0L)
TRIETHYLAMINE (UNII: VOU728O6AY)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)

Product Characteristics
Color		Score
Shape	BULLET	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 41878-002-01	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/16/2020

Labeler - Guangzhou Youmei Biotechnology Co., Ltd. (418782063)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Youmei Biotechnology Co., Ltd.		418782063	manufacture(41878-002)