Antibacterial Wet Wipes by Positive Promotions Inc. Antibacterial Wet Wipes

Antibacterial Wet Wipes by

Drug Labeling and Warnings

Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Positive Promotions Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth 
Positive Promotions Inc.

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Antibacterial Wet Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antiseptic

Uses

  • For hand-washing to decrease bacteria on skin

WARNING

Flammable. Keep away from heat and flame.

For External use only.

Do not use

in eyes. In case of contact, rinse thoroughly with water.

Stop use & ask doctor

if rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep out of reach of children

except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. 
  • Thoroughly wipe hands, allow to dry out rinsing. 
  • Discard after single use 

Other information

  • Do not flush down toilet. 
  • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)
  • May discolor certain fabrics

Inactive Ingredients

Water, Phenoxyethanol, Ethylhexyl Glycerin, Didecyldimonium Chloride, Propylene Glycol, Glycerin, Fragrance.

Package Labeling:

Label

ANTIBACTERIAL WET WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79021-007(NDC: 77796-210)
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79021-007-1515 in 1 POUCH10/01/202011/30/2023
13.5 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 Drug505G(a)(3)10/01/202011/30/2023
Labeler - Positive Promotions Inc. (002401719)

Revised: 1/2024