BioPure Antibacterial Hand Wipes

BioPure Antibacterial Hand Wipes by

Drug Labeling and Warnings

BioPure Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by QUEST USA CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BIOPURE ANTIBACTERIAL HAND WIPES- alcohol cloth 
QUEST USA CORP.

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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BioPure Antibacterial Hand Wipes

Drug Facts

Active ingredient

Ethyl Alcohol 75%

Purpose

Antibacterial

Uses

  • Hand sanitizer to help reduce bacteria.
  • For use when soap and water are not available.

Warnings

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

Do not use

  • in children less than 2 months of age.
  • on open skin wounds.

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 rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply to hands, allow to air dry without wiping.
  • Children under 6 years of age should be supervised when using this product.

Other Information

  • Store in a cool, dry place, between 15°-30°C (59°F-86°F).
  • Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredient

Purified water USP

Questions?

call 718-975-2586

Package Labeling:

Bottle

BIOPURE ANTIBACTERIAL HAND WIPES 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78691-016
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 78691-016-01100 in 1 CANISTER11/15/202012/31/2022
15.4 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/15/202012/31/2022
Labeler - QUEST USA CORP. (079869689)

Revised: 12/2022
 

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