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Personal CARE Antibacterial Foaming Hand Wild Flowers

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.0002218mg in 221.8mL
Labeler: Personal Care Products, LLC
NDC Code: 29500-9881

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.

Personal CARE Antibacterial Foaming Hand Soap
Wild Flowers - Fresh Picked Strawberries - Beach Breeze - Citrus Sunshine

Drug Facts
Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Keep out of reach of children

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

Uses

for hand washing to decrease bacteria on the skin.

Warnings

For external use only.

When using this product

avoid contact with eyes. In case of eye contact, flush with clean water.

Stop use and ask a doctor

if irritation and redness develops.

Directions
  • pump into hands
  • lather vigorously for at least 15 seconds
  • rinse and dry thoroughly.

Inactive ingredients

Water (Aqua), Laureth-9, Disodium, Cocoamphodiacetate, Citric Acid, Fragrance, Glycerin, Methylchloroisothiazolinone, Methylisothiazolinone.

Personal CARE ® ANTIBACTERIAL FOAMING Hand Soap Labels
Wild Flowers
Fresh Picked Strawberries
Breach Breeze
Citrus Sunshine

Personal CARE ® ANTIBACTERIAL FOAMING Hand Soap

Wild Flowers
Fresh Picked Strawberries
Breach Breeze
Citrus Sunshine

TRICLOSAN FREE
7.5 FL OZ (221.8 mL)

Distributed by: PERSONAL CARE PRODUCTS, LLC

3001 Big Beaver Rd, Ste 520 Troy, MI 43034

Made in China

PERSONAL CARE ANTIBACTERIAL  FOAMING HAND WILD FLOWERS
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9881
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.0002218 mg  in 221.8 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
LAURETH-9 
DISODIUM COCOAMPHODIACETATE 
CITRIC ACID MONOHYDRATE 
GLYCERIN 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:29500-9881-1221.8 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/10/2015
PERSONAL CARE ANTIBACTERIAL  FOAMING HAND FRESH PICKED STRAWBERRIES
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9018
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.0002218 mg  in 221.8 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
LAURETH-9 
DISODIUM COCOAMPHODIACETATE 
CITRIC ACID MONOHYDRATE 
GLYCERIN 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:29500-9018-1221.8 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/10/2015
PERSONAL CARE ANTIBACTERIAL  FOAMING HAND BEACH BREEZE
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9020
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.0002218 mg  in 221.8 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
LAURETH-9 
DISODIUM COCOAMPHODIACETATE 
CITRIC ACID MONOHYDRATE 
GLYCERIN 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:29500-9020-1221.8 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/10/2015
PERSONAL CARE ANTIBACTERIAL  FOAMING HAND CITRUS SUNSHINE
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29500-9319
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.0002218 mg  in 221.8 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
LAURETH-9 
DISODIUM COCOAMPHODIACETATE 
CITRIC ACID MONOHYDRATE 
GLYCERIN 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
Packaging
#Item CodePackage Description
1NDC:29500-9319-1221.8 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/10/2015
Labeler - Personal Care Products, LLC (966155082)
Registrant - Personal Care Products, LLC (966155082)

Revised: 12/2015
 
Personal Care Products, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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