FRST1 ALCOHOL WIPES- alcohol wipes cloth

FRST1 ALCOHOL WIPES by

Drug Labeling and Warnings

FRST1 ALCOHOL WIPES by is a Otc medication manufactured, distributed, or labeled by LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable, keep away from heat and flames.

When using this product, Avoid contact with eyes.

In case of contact with eyes, rinse eyes thoroughly with water.

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

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

WHEN USING

When using this product, Avoid contact with eyes.

In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation 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

Open the resealable sticker on the top and remove a wipe for use. When needed, rub/wipe vigorously on hands, between fingers, at fingernails, and then scrub wrists and forearms. After use, reseal the sticker on top to avoid evaporation of alcohol.

Other Information

Dispose of wipe in the proper receptacle.

Do not flush down the toilet.

Store between 59-86 F (15-30 C).

Inactive Ingredient

Water

PRINCIPAL DISPLAY PANEL

50 WIPES, NDC: 75269-007-01

INGREDIENTS AND APPEARANCE

FRST1 ALCOHOL WIPES 
alcohol wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75269-007
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
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75269-007-01	50 in 1 BAG	11/26/2020
1		4 mL in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/26/2020

Labeler - LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD. (560972943)

Registrant - LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD. (560972943)

Establishment
Name	Address	ID/FEI	Business Operations
LINGHAI ZHANWANG BIOTECHNOLOGY CO.,LTD.		560972943	manufacture(75269-007)