Label: DERM-APPLY- glycerin 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 November 23, 2010

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  • ACTIVE INGREDIENT

    GLYCERIN

  • INACTIVE INGREDIENTS

    DEIONIZED WATER, PETROLATUM, MINERAL OIL, SODIUM LAURYL SULFATE, METHYLPARABEN, PROPYLPARABEN

  • PURPOSE

    RESTORE MOISTURE BALANCE IN DRY SKIN OR HAIR

  • USE

    CONCENTRATED, FOR EXTERNAL USE ONLY

  • KEEP OUT OF REACH OF CHILDREN

    Enter section text here

  • DIRECTIONS

    SHAKE WELL BEFORE USING

    FOR BEST RESULTS, WASH OR WET AREA WITH WATER AND PAT DRY.  APPLY A SMALL AMOUNT - 5 TO 10 DROPS OF CONCENTRATED DERM-APPLY MOISTURIZING LOTION AND RUB IN THOROUGHLY. 

  • WARNINGS

    FOR EXTERNAL USE ONLY.  SHAKE WELL BEFORE USING

  • DERM-APPLY LABEL

    DERM-APPLY tm  MOISTURIZING LOTION

    CONCENTRATED TO QUICKLY RESTORE MOISTURE BALANCE IN DRY SKIN OR HAIR

    MANUFACTURED BY SNUVA, INC  715 SOUTH BLVD OAK PARK, IL 60302


    DERM-APPLY SENTED FRONT


    DERM-APPLY SENTED BACK


    DERM-APPLY UNSENTED FRONT

    DER-APPLY UNSENTED BACK

  • INGREDIENTS AND APPEARANCE
    DERM-APPLY 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58291-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN30.78 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ROSE OIL (UNII: WUB68Y35M7)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58291-0001-159 mL in 1 BOTTLE
    2NDC:58291-0001-2177 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33401/01/1989
    Labeler - Snuva, Inc. (807310008)
    Registrant - Snuva, Inc. (807310008)
    Establishment
    NameAddressID/FEIBusiness Operations
    Snuva, Inc.807310008manufacture
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