Sanko Sanitizing Wipes by Harper + Scott LLC Sanko Sanitizing Wipes

Sanko Sanitizing Wipes by

Drug Labeling and Warnings

Sanko Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Harper + Scott LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SANKO SANITIZING WIPES- alcohol cloth 
Harper + Scott LLC

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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Sanko Sanitizing Wipes

Drug Facts

Active Ingredient

Alcohol 70% v/v

Purpose

Antiseptic

Use For sanitizing to decrease bacteria on the skin. For use when soap and water are not available.

Warnings

For external use only.

Flammable, keep away from fire or flame.

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Discontinue use if irritation and redness develops. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 1-800-222-1222

Directions

• Open packet, remove and unfold pre-moistened tissue.
• Wipe hands and allow to dry without wiping.
• Discard properly after single use.
• Do not flush down toilet.

Other Information

• Store at room temperature. Keep out of direct sunlight.

Inactive Ingredients

Water, Glycerol.

Made in China.

Distributed by Harper and Scott, LLC

915 Broadway New York, NY 10010

www.shopsanko.com

Kills most germs without water. Personal safety for every person.

100 Soft Wipes: 7.87" x 5.90" (20 cm x 15 cm)

This product is made of spunlaced non-woven fabric and should not be flushed down the toilet into any sewer system.

SANKO

Sanitizing Wipes

Fragrance Free

Antibacterial Disposable Wipes

Alcohol Antiseptic 70%

100 Soft Wipes

SANKO SANITIZING WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80744-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80744-001-01	100 in 1 POUCH	10/02/2020	10/29/2021
1		4.2 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/02/2020	10/29/2021

Labeler - Harper + Scott LLC (077459979)

Revised: 10/2021

Document Id: cf83ea71-d61d-03a3-e053-2995a90a727a

34390-5

Set id: b0b2814c-517d-a2e0-e053-2a95a90adc4c

Version: 2

Effective Time: 20211029