Label: DG DEEP CLEANING ASTRINGENT SENSITIVE SKIN- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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.

Drug Label Information

Updated December 7, 2012

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  • PRINCIPAL DISPLAY PANEL

    DRUG FACTS

    Active Ingredient

    Salicylic acid 0.50%

    USE for treatment of acne

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

  • INDICATIONS & USAGE

    USE FOR TREATMENT OF ACNE

  • WARNINGS

    FOR EXTERNAL USE ONLY, Flammable, keep awat from open fire or flame, Using other topical acne medication at the same time or immediately following the use fo this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Rinse right away with water if it gets in eyes.

  • DOSAGE & ADMINISTRATION

    • CLEANSE SKIN THOROUGHLY BEFORE APPLYING MEDICATION
    • MOISTEN A COTTON BALL AND COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER 1 TO 3 TIMES DAILY
    • BECAUSE EXCESSIVE DRYING OF THE SKIN MAY OCCUR, START WITH 1 APPLICATION DAILY. THEN GRADUALLY INCREASE TO 2 OR 3 TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCOR. IF BOTHERSOME DRYING OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.
  • INACTIVE INGREDIENT

    WATER, Alcohol, Glycerin, Isoceteth-20, Sodium Citrate, Fragrance, Propylene Glycol, Benzophenone-4, Algae extract, Aloe barbadensis leaf extract, triethanolamine, denatonium benzoate, blue 1

  • PRINCIPAL DISPLAY PANEL

    IMAGE OF FRONT LABELIMAGE OF BACK LABEL

  • INGREDIENTS AND APPEARANCE
    DG DEEP CLEANING ASTRINGENT SENSITIVE SKIN 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60742-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOCETETH-20 (UNII: O020065R7Z)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZOPHENONE (UNII: 701M4TTV9O)  
    ALOE (UNII: V5VD430YW9)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60742-002-01240 g in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333D01/31/2013
    Labeler - BELVEDERE INTERNATIONAL INC. (247836356)
    Registrant - BELVEDERE INTERNATIONAL INC. (247836356)
    Establishment
    NameAddressID/FEIBusiness Operations
    BELVEDERE INTERNATIONAL INC.247836356manufacture(60742-002)
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