Dr. Ato Hand Sanitizing Wipes

Dr. Ato Hand Sanitizing Wipes by

Drug Labeling and Warnings

Dr. Ato Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by HANUL CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. ATO HAND SANITIZING WIPES- alcohol cloth 
HANUL CO., LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dr. Ato Hand Sanitizing Wipes

Active Ingredient(s)

Alcohol 62% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizing Wipes

Use

To decrease bacteria on the skin that could cause disease.

Warnings

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

Do not use

Not recommended for infants

When using the product, Keep oyut of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Donot inhale or ingest.

Stop use and ask a doctor if irritation or redness develops condition persists for more than 72 hours.

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

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Other information

• Do not store above 105F/40C
• May discolor some fabrics
• Harmful to wooden finishes and plastics

Inactive ingredients

Water, Butylene Glycol, Sodium Benzoate, Citric Acid

Package Label - Principal Display Panel

NDC: 75214-278-34

Dr. Ato Hand Sanitizing Wipes

NON STERILE SOLUTION

62% ALCOHOL ANTISEPTIC

reduce bacteria that potentially can cause disease

50 wipes

wipes dimension 6in. x 8 in. (15cm x 20cm)

DR. ATO HAND SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75214-278
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.25 mL  in 100 mL
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	1 mL  in 100 mL
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.3 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75214-278-34	334 mL in 1 PACKET; Type 0: Not a Combination Product	06/23/2020	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/23/2020	12/31/2021

Labeler - HANUL CO., LTD (557814370)

Revised: 1/2022

Document Id: d4b133a4-13de-49e1-e053-2995a90ab4ef

34390-5

Set id: a8ad3189-e2f6-d4ef-e053-2995a90a60e0

Version: 3

Effective Time: 20220103