TRICLOSAN by CVS Pharmacy / Pharma Pac, LLC TRICLOSAN liquid

TRICLOSAN by

Drug Labeling and Warnings

TRICLOSAN by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Pharma Pac, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                      Purpose
Triclosan 0.25%...............................Antiseptic

PURPOSE

Active ingredient                       Purpose

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

Use to decrease bacteria on the skin

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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

Smooth over face and neck. Rinse thoroughly.

WARNINGS

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.

DOSAGE & ADMINISTRATION

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 INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TRICLOSAN 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-081
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (UNDECYLENIC ACID - UNII:K3D86KJ24N)	TRICLOSAN	29 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)	712 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-081-20	240 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2008

Labeler - CVS Pharmacy (062312574)

Registrant - Pharma Pac, LLC (140807475)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Pac, LLC		140807475	manufacture