Label: ABOVE INTIMATE LIQUIDSOAP- above intimate liquid

  • NDC Code(s): 73306-1161-1
  • Packager: BASTON INDUSTRIA DE AEROSSOIS LTDA
  • 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 August 15, 2023

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    ALOE BARBADENSIS EXTRACT (EXTRATO DE ALOE VERA) CONDICIONADOR DA PELE 0.1

  • INACTIVE INGREDIENT

    AQUA (ÁGUA)
    SODIUM LAURETH SULFATE (LAURILETERSULFATO DE SÓDIO)
    GLYCERIN (GLICEROL)
    PALM KERNELAMIDE DEA (PALMISTAMIDA DEA)
    POLYQUATERNIUM-7 (POLIQUATÉRNIO-7)
    COCAMIDOPROPYL BETAINE (COCOAMIDOPROPIL BETAÍNA)
    PARFUM (PERFUME)
    DIPROPYLENE GLYCOL (DIPROPILENOGLICOL)
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (CLORETO DE GUAR HIDROXIPROPILTRIMÔNIO)
    PHENYLPROPANOL (FENILPROPANOL)
    PENTYLENE GLYCOL (PENTILENOGLICOL)
    LACTIC ACID (ÁCIDO LÁTICO)
    1,2-HEXANEDIOL (1,2-HEXANODIOL)
    PROPYLENE GLYCOL (PROPILENOGLICOL)
    ALPHA-GLUCAN OLIGOSACCHARIDE (OLIGOSSACARÍDEO DE ALFA-GLUCANA)
    C10-16 ALKETH-2 (C-10-16-ALQUETE-2)
    SODIUM CHLORIDE (CLORETO DE SÓDIO)
    SODIUM SULFATE (SULFATO DE SÓDIO)
    SODIUM GLUCONATE (GLUCONATO DE SÓDIO)
    BUTETH-3 (BUTETE-3)
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (BENZOTRIAZOLIL BUTILFENOL SULFONATO DE SÓDIO)
    SODIUM CITRATE (CITRATO DE SÓDIO)
    BENZOIC ACID (ÁCIDO BENZÓICO)
    TRIBUTYL CITRATE (CITRATO DE TRIBUTILA)
    CITRIC ACID (ÁCIDO CÍTRICO)

  • PURPOSE

    SOAP FOR INTIMATE USE

  • WARNINGS AND PRECAUTIONS

    KEEP OUT OF REACH OF CHILDREN AND PETS. EXTERNAL USE.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • DOSAGE & ADMINISTRATION

    APPLY TO THE PREVIOUSLY MOISTENED EXTERNAL INTIMATE REGION. SPREAD UNTIL FOAMY. RINSE THOROUGHLY AFTER USE

  • QUESTIONS

    MAIL : SUPPORT@MYSPRAY.GROUP OR CALL (305) 677-5030

  • INDICATIONS & USAGE

    APPLY TO THE PREVIOUSLY MOISTENED EXTERNAL INTIMATE REGION. SPREAD UNTIL FOAMY. RINSE THOROUGHLY AFTER USE

  • WARNINGS

    KEEP OUT OF REACH OF CHILDREN AND PETS. EXTERNAL USE.

  • PRINCIPAL DISPLAY PANEL

    LABEL

  • INGREDIENTS AND APPEARANCE
    ABOVE INTIMATE LIQUIDSOAP 
    above intimate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73306-1161
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9) ALOE0.01 mg  in 250 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH-2 SULFATE (UNII: ZZQ59TY3KG)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73306-1161-1250 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM00308/15/2023
    Labeler - BASTON INDUSTRIA DE AEROSSOIS LTDA (897727605)
    Registrant - BASTON INDUSTRIA DE AEROSSOIS LTDA (897727605)
    Establishment
    NameAddressID/FEIBusiness Operations
    BASTON INDUSTRIA DE AEROSSOIS LTDA897727605manufacture(73306-1161)