CVS DEEP CLEANSING ASTRINGENT- salicylic acid liquid

CVS Deep Cleansing Astringent by

Drug Labeling and Warnings

CVS Deep Cleansing Astringent 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

Salicylic Acid 0.5%.........................................Acne medication

PURPOSE

Uses for the treatment of acne

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

Uses for the treatment of acne 

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 medications 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 the 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

Other information store at room temperature
 

INACTIVE INGREDIENT

Inactive Ingredients


alcohol, alge extract, aloe barbadensis leaf extract, benzophenone-4, blue-1,
dentatonium benzonate, dimethicone propyl PG-betaine, fragrance, glycerin,
isoceteth-20, PEG-32, propylene glycol, purified water, sodium citrate 

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS DEEP CLEANSING ASTRINGENT 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-811
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZOPHENONE (UNII: 701M4TTV9O)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
GLYCERIN (UNII: PDC6A3C0OX)
ISOCETYL ALCOHOL (UNII: 1800H64066)
PEG-32 STEARATE (UNII: 33GX5WQC0M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-811-31	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