ALCOHOL WIPES- alcohol cloth

Alcohol Wipes by

Drug Labeling and Warnings

Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Shaoxing Elite Bio-Tech Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

Alcohol 75% v/v

Purpose

Antiseptic

Use

For hand sanitizing to decrease bacteria on skin.

Warnings

For external use only. Flammable: Keep away from fire or flame.

Do not use

In children less than 2 months of age.

On open skin wounds.

WHEN USING

When using this product avoid contact with eyes and mouth. If in eyes，flush thoroughly with water.

STOP USE

Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

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

Directions

Open the lid, tear open packet, remove wipe.

Wet hands thoroughly with product and let hands air dry.

Throw used wipe in trash.

Do not flush.

Other information

Store between 15-30 °C (59-86 °F).

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

Inactive ingredients

Water.

Package Label - Principal Display Panel

NDC: 81079-002-01

NDC: 81079-002-02

NDC: 81079-002-03

NDC: 81079-002-04

NDC: 81079-002-05

NDC: 81079-002-06

INGREDIENTS AND APPEARANCE

ALCOHOL WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81079-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81079-002-01	38 mL in 1 BAG; Type 0: Not a Combination Product	11/16/2020
2	NDC: 81079-002-02	76 mL in 1 BAG; Type 0: Not a Combination Product	11/16/2020
3	NDC: 81079-002-03	153 mL in 1 BAG; Type 0: Not a Combination Product	11/16/2020
4	NDC: 81079-002-04	230 mL in 1 BAG; Type 0: Not a Combination Product	11/16/2020
5	NDC: 81079-002-05	307 mL in 1 BAG; Type 0: Not a Combination Product	11/16/2020
6	NDC: 81079-002-06	384 mL in 1 BAG; Type 0: Not a Combination Product	11/16/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/16/2020

Labeler - Shaoxing Elite Bio-Tech Co.,Ltd. (546459425)

Registrant - Shaoxing Elite Bio-Tech Co.,Ltd. (546459425)

Establishment
Name	Address	ID/FEI	Business Operations
Shaoxing Elite Bio-Tech Co.,Ltd.		546459425	manufacture(81079-002)