Antibacterial Wipes by Positive Promotions Inc. Antibacterial Wipes

Antibacterial Wipes by

Drug Labeling and Warnings

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

Drug Details [pdf]

ANTIBACTERIAL WIPES- benzalkonium chloride cloth 
Positive Promotions Inc.

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Antibacterial Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antibacterial

Uses

  • For hand-washing to decrease bacteria on skin

Warnings

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 from children

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

Directions

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.
  • Thoroughly wipe hands, allow to dry without rinsing.
  • Discard after single use
  • Use within a month of opening

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

Proylene Glycol, Aqua, Kathon, Tocopherol, Fragrance

Package Labeling:60 count

Box

ANTIBACTERIAL WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79021-004
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
OCTHILINONE (UNII: 4LFS24GD0V)  
TOCOPHEROL (UNII: R0ZB2556P8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79021-004-6060 in 1 CASE09/01/202011/30/2023
11.5 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)09/01/202011/30/2023
Labeler - Positive Promotions Inc. (002401719)

Revised: 10/2023