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TRICLOSAN by CVS Pharmacy

Dosage form: liquid
Ingredients: TRICLOSAN 29mg in 1mL
Labeler: CVS Pharmacy
NDC Code: 59779-081

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                      Purpose
Triclosan 0.25%...............................Antiseptic



Active ingredient                       Purpose

Triclosan 0.25%...............................Antiseptic

Use to decrease bacteria on the skin


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



Directions mix in hands with water. Work into a foamy lather.

Smooth over face and neck. Rinse thoroughly.


Warnings For external use only.


Stop use and ask a doctor if


- excessive skin irritation develops or condition worsens
- symptoms last more than 7 days or clear up and occur
again within a few days.

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


Directions
- Mix in hands with water. Work into a foamy lather.
Smooth over face and neck. Rinse thoroughly.

Other Information do not store in a location where water may enter the bottle




Inactive Ingredients BHT, Butylparaben, C9-15 Alkyl Phosphate,
Cocamidopropyl Bataine, Ethylparaben, Fragrance, Glycerin,
Hydroxypropyl Methylcelluose, Lauric Acid, Methylparaben, Myristic Acid,
Phenoxyethanol, Propylparaben, Triethanolamine, Water, Red 40, Yellow 10



TRICLOSAN 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-081
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNDECYLENIC ACID) TRICLOSAN29 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL PALMITATE712 mg  in 1 mL
Packaging
#Item CodePackage Description
1NDC:59779-081-20240 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/2008
Labeler - CVS Pharmacy (062312574)
Registrant - Pharma Pac, LLC (140807475)
Establishment
NameAddressID/FEIOperations
Pharma Pac, LLC140807475manufacture

Revised: 02/2011
 
CVS Pharmacy

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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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