ADVANCED ACNE SPOT TREATMENT CVS- salicylic acid 2.00% lotion

Advanced Acne Spot Treatment by

Drug Labeling and Warnings

Advanced Acne Spot Treatment by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient                          Purpose

Salicylic Acid – 2.00%                  Acne Medication

PURPOSE

Use

For treatment of acne

WarningsFor external use only

​Flammable. Keep away from fire or flame.

​When using this product and other topical acne medications at the same time or immediately following use of this product, increased dryness or irritation of the skin may occur. If this occurs, only one medication should be used unless directed by a doctor.

Keep out of reach of the children
If product is swallowed, get medical help or contact a Poison Control Center right away. Avoid contact with eyes. If contact occurs, flush thoroughly with water

DOSAGE & ADMINISTRATION

Directions ​ cleans the skin thoroughly before applying medication cover the entire affected area with a thin layer one to three times a day If bothersome dryness or peeling occurs, reduce application to once a day or every other day. Recomended for daily use.

INACTIVE INGREDIENT

Inactive ingredients :Water, Alcohol, Hamamelis Virginiana (Witch Hazel) Extract, Glycerin, C13-14 Isoparaffin, Laureth-7, Polyacrylamide
C12-15 Alkyl Lactate, Cetyl Lactate, Cedrus Atlantica Bark Extract, Cinnamomum Zeylanicum Bark Extract, Butylene Glycol, Dimethicone, Capryloyl Glycine, Ammonium Hydroxide, Portulaca Oleracea Extract, Benzalkonium Chloride, Propylene Glycol, Cocamidopropyl PG-Dimonium , hloride Phosphate, Cyclopentasiloxane, Phenoxyethanol, Dehydroxanthan Gum, Denatonium Benzoate, Fragrance, Hexylene Glycol, Polysorbate 20, PPG-2 Isoceteth-20 Acetate, Sarcosine, t-Butyl Alcohol, Tetrasodium EDTA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ADVANCED ACNE SPOT TREATMENT  CVS
salicylic acid 2.00% lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-343
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	Salicylic Acid	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alcohol (UNII: 3K9958V90M)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
Glycerin (UNII: PDC6A3C0OX)
C13-14 Isoparaffin (UNII: E4F12ROE70)
Laureth-7 (UNII: Z95S6G8201)
C12-15 Alkyl Lactate (UNII: GC844VRD7E)
Cetyl Lactate (UNII: A7EVH2RK4O)
CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)
CINNAMON BARK OIL (UNII: XE54U569EC)
Butylene Glycol (UNII: 3XUS85K0RA)
Capryloyl Glycine (UNII: 8TY5YO42NJ)
AMMONIA (UNII: 5138Q19F1X)
PURSLANE (UNII: M6S840WXG5)
Benzalkonium Chloride (UNII: F5UM2KM3W7)
Propylene Glycol (UNII: 6DC9Q167V3)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Dehydroxanthan Gum (UNII: 63ZP7I1BQO)
Denatonium Benzoate (UNII: 4YK5Z54AT2)
Polysorbate 20 (UNII: 7T1F30V5YH)
PPG-2 Isoceteth-20 Acetate (UNII: BI6C7YO419)
Sarcosine (UNII: Z711V88R5F)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
EDETATE SODIUM (UNII: MP1J8420LU)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-343-01	1 in 1 CARTON	12/22/2014
1		22 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	12/22/2014

Labeler - CVS (062312574)

Registrant - Product Quest Mfg. (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg.		927768135	manufacture(59779-343) , label(59779-343)