Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

Drug Labeling and Warnings

Drug Details

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AFIA ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride soap 
National Chemical Laboratories, Inc.

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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Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

Drug Facts

Active Ingredient. Purpose

Benzalkonium Chloride 0.1%...........Antimicrobial

Active Ingredient. Purpose Benzalkonium Chloride 0.1%...........Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings:

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

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

Directions

  • Pump a small amount of foam into palm of hand
  • Rub thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry

Inactive ingredients

Water, dihyroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Uses

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use

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

Afia Alcohol-Free Foaming Hand Sanitizer

Afia Alcohol-Free Foaming Hand Sanitizer

Afia Alcohol-Free Foaming Hand Sanitizer

Afia Alcohol-Free Foaming Hand Sanitizer

AFIA ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 71023-445
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 71023-445-571000 mL in 1 BAG; Type 0: Not a Combination Product10/24/2016
2NDC: 71023-445-293785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/24/2016
Labeler - National Chemical Laboratories, Inc. (002289619)
Registrant - National Chemical Laboratories, Inc. (002289619)
Establishment
NameAddressID/FEIBusiness Operations
National Chemical Laboratories, Inc.002289619manufacture(71023-445)

Revised: 3/2020
 
National Chemical Laboratories, Inc.


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