Label: VIPER ACNE BODY WASH- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 March 18, 2011

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  • ACTIVE INGREDIENT

    SALICYLIC ACID 2%

  • PURPOSE

    ACNE TREATMENT

    USES

    FOR THE TREATMENT OF ACNE.  HELPS PREVENT THE DEVELOPMENT OF NEW ACNE BLEMISHES.

  • WARNINGS

    FOR EXTERNAL USE ONLY.

    WHEN USING THIS PRODUCT

    AVOID CONTACT WITH EYES.  IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER.

    USING OTHER TOPICAL ACNE DRUGS AT THE SAME TIME OR RIGHT AFTER USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN.  IF THIS OCCURS, ONLY ONE DRUG SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

    STOP USING THIS PRODUCT AND ASK A DOCTOR IF

    IRRITATION OR RASH DEVELOPS AND LASTS.

    KEEP OUT OF REACH OF CHILDREN

    Enter section text here

  • DIRECTIONS:

    Enter section text here

  • INACTIVE INGREDIENTS

    WATER, SODIUM LAURETH SULFAE, SODIUM C14-16 OLEFIN SULFONATE, COCAMIDOPROPYL BETAINE, SODIUM C12-15 PARETH-15 SULFONATE, FRAGRANCE, CITRIC ACID, LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, PROPYLENE GLYCOL, DECYLENE GLYCOL, ALOE BARBADENSIS LEAF EXTRACT, ANTHEMIS NOBILIS FLOWER EXTRACT, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, SODIUM CHLORIDE, BLUE 1 (CI 42090), EXT.VIOLET 2 (CI 60730).

  • PRINCIPAL DISPLAY PANEL

    IMAGE OF VIPER

  • INGREDIENTS AND APPEARANCE
    VIPER ACNE BODY WASH 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-806
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM C12-15 PARETH-15 SULFONATE (UNII: 353VA59XH8)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    1-DECENE (UNII: 7O4U4C718P)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    CHAMOMILE (UNII: FGL3685T2X)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-806-12354 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D03/18/2011
    Labeler - CVS PHARMACY (062312574)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture
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