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Antibacterial Foam with Moisturizers

Dosage form: soap
Ingredients: TRICLOSAN 0.3mg in 100mL
Labeler: Chester Packaging, LLC
NDC Code: 12462-502

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.

Drug Facts

Active ingredient

Triclosan 0.3%

Purpose

Antimicrobial

Uses
  • Handwash to help reduce bacteria that potentially can cause disease.

Warnings
  • For external use only.

Ask a doctor before use if you have
  • Deep wounds, animal bites or serious burns.

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

Stop use and ask a doctor if
  • irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.
  • If swallowed, seek immediate medical attention or call a Poison Control Center right away.

Directions
  • Wet hands, apply foam, lather for 30 seconds and rinse hands thoroughly.

Inactive ingredients

Water, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Propylene Glycol, Lauramide DEA, Cocamide DEA, Cocamidopropyl Betaine, Glycerine, Polyquaternium-7, Sodium Chloride, Sodium Cumenesulfonate, Citric Acid, DMDM Hydantoin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothazolinone, Aloe Barbadensis Leaf Juice, and Tocopherol Acetate.

Package Label Principal Display Panel

48212

Foam Antibacterial Soap with Moisturizers

No Fragrance Added

Product Dispenser Label

Foam Antibacterial Soap with Moisturizers

No Fragrance Added

Pacific Garden

1200 mL (40.8 fl. oz.)

ANTIBACTERIAL FOAM  WITH MOISTURIZERS
triclosan soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12462-502
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN0.3 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
SODIUM LAURYL SULFATE 
PROPYLENE GLYCOL 
LAURIC DIETHANOLAMIDE 
COCAMIDE DIETHANOLAMINE 
COCAMIDOPROPYL BETAINE 
GLYCERIN 
SODIUM CHLORIDE 
CITRIC ACID MONOHYDRATE 
DMDM HYDANTOIN 
EDETATE SODIUM 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
ALOE VERA LEAF 
.ALPHA.-TOCOPHEROL ACETATE, D- 
Packaging
#Item CodePackage Description
1NDC:12462-502-124 BOTTLE (BOTTLE) in 1 CASE
11200 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33301/01/2007
Labeler - Chester Packaging, LLC (004237806)

Revised: 05/2010
 
Chester Packaging, 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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