- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
Warnings
For external use only
Flammable: Keep away from fire or flame
When using this product
- avoid contact with eyes. If contact occurs, flush thoroughly with water.
- using other topical acne medication at the same time or right after use of this product,
may increase dryness or irritation of the skin. If this occurs, only one medication should
be used unless directed by a doctor.
Keep out of reach of children.If swallowed, get medical help or contact a
Poison Control Center right away. -
DOSAGE & ADMINISTRATION
Directions
- cleanse skin thoroughly before applying medication
- moisten cotton ball or pad and pat over face and neck
- because too much drying of teh skin may occur, start with 1 application daily,
then gradually increase to 2 to 3 times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- to prevent discoloration of clothing, avoid contact
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
CVS TRIPLE ACTION ASTRINGENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-807 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) ISOPROPYL ALCOHOL (UNII: ND2M416302) POLYSORBATE 60 (UNII: CAL22UVI4M) MENTHOL (UNII: L7T10EIP3A) SODIUM CITRATE (UNII: 1Q73Q2JULR) BENZOPHENONE (UNII: 701M4TTV9O) EDETATE DISODIUM (UNII: 7FLD91C86K) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) GLYCERIN (UNII: PDC6A3C0OX) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-807-62 250 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 07/08/2010 Labeler - CVS Pharmacy (062312574) Registrant - Pharma Pac, LLC (140807475) Establishment Name Address ID/FEI Business Operations Pharma Pac, LLC 140807475 manufacture