Alcohol Wipe by YAHON ENTERPRISE CO.,LTD Yahon 001-08

Alcohol Wipe by

Drug Labeling and Warnings

Alcohol Wipe by is a Otc medication manufactured, distributed, or labeled by YAHON ENTERPRISE CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALCOHOL WIPE- alcohol cloth 
YAHON ENTERPRISE CO.,LTD

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Yahon 001-08

Active Ingredient(s)

Alcohol 75%. Purpose: Antiseptic

Purpose

Antiseptic

Use

To decrease bacteria on the skin

Recommended for repeated use

Warnings

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

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 redness develop or last more than 72 hours

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

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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

Directions

Rub wire thoroughly over all surfaces of both hands and allow to dry.

Supervise children under 6 years old.

Not recommended for infants

Discard wipe in trash; do not flush

Inactive ingredients

Benzalkonium Chloride, Citric Acid, Polyaminopropyl Biguanide Water

Package Label - Principal Display Panel

50 wipes NDC: 79618-001-08

ALCOHOL WIPE 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79618-001
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

Inactive Ingredients
Ingredient Name	Strength
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
CITRIC ACID ACETATE (UNII: DSO12WL7AU)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79618-001-08	50 in 1 PACKET; Type 0: Not a Combination Product	10/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/31/2020	10/01/2024

Labeler - YAHON ENTERPRISE CO.,LTD (555347945)

Establishment
Name	Address	ID/FEI	Business Operations
YAHON ENTERPRISE CO.,LTD		555347945	manufacture(79618-001)

Revised: 10/2024

Document Id: 236fc9b0-64da-88cd-e063-6394a90a06a8

34390-5

Set id: b3038abe-4d70-d97e-e053-2995a90aeee8

Version: 6

Effective Time: 20241001