PURE FORMULA 1 ADVANCED ALCOHOL WIPES 01- alcohol cloth

Pure Formula 1 advanced alcohol wipes by

Drug Labeling and Warnings

Pure Formula 1 advanced alcohol wipes by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Science Co.,Ltd., Lantern Beauty America,Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

drug facts

Active ingredient

Active ingredient purpose

Ethyl alcohol 75%v/v Antiseptic

Use

for hand-washing to help reduce bacteria that potentially can cause disesase.For use when soap and waterare not available.

warnings

For external use only.Flammable.Keep away from heat or flame.

Do not use

in children less than 2 months of age

on open skin wounds.

When using this product

Keep out of eyes,ears,and mouth.In case of contact with eyes,rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs,these maybe signs of a serious condition.

Keep out of reach of children

if swallowed,get medical help or contact a Poison Control Center right away.

Directions

Place enough product on hands to cover all surfaces,Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing

Other information

Store between15-30C(59-86F)

Avoid freezing and excessive heat above 40C(104F)

Inactive ingredient

Water(25%)

usage

Place enough product on hands to cover all surfaces,Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PURE FORMULA 1 ADVANCED ALCOHOL WIPES  01
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-298
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75   in 100

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	25

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-298-01	50 in 1 PACKAGE; Type 0: Not a Combination Product	08/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/03/2020

Labeler - Shenzhen Lantern Science Co.,Ltd. (421222423)

Registrant - Lantern Beauty America,Inc. (117371139)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co.,Ltd.		421222423	manufacture(54860-298)