ADVANCED ACNE SPOT TREATMENT CVS- salicylic acid 2.00% lotion 
CVS

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.

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Active ingredient                          Purpose

Salicylic Acid – 2.00%                  Acne Medication

Use

For treatment of acne

Warnings
For 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

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 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

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ADVANCED ACNE SPOT TREATMENT  CVS
salicylic acid 2.00% lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-343
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) Salicylic Acid2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-343-011 in 1 CARTON12/22/2014
122 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D12/22/2014
Labeler - CVS (062312574)
Registrant - Product Quest Mfg. (927768135)
Establishment
NameAddressID/FEIBusiness Operations
Product Quest Mfg.927768135manufacture(59779-343) , label(59779-343)

Revised: 12/2017
Document Id: 495e462d-4721-43fa-87b6-e7386ddd0338
Set id: 439e6506-40a6-4dce-80db-11dbe6d55fc3
Version: 2
Effective Time: 20171226
 
CVS