Label: WHP BE GONE SCRATCH-N-ITCH TM (grindelia squarrosa flowering top - camphor- natural spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated August 2, 2013

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

  • ACTIVE INGREDIENTS

    GRINDELIA

    CAMPHOR

  • USES

    Relief from itchy skin.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS

    Indications:

    GRINDELIA   Rash

    CAMPHOR    Coldness

  • STOP USE AND ASK DOCTOR

    For external use only. If symptoms persist/worsen or if pregnant/nursing, consult your practitioner. Do not use if seal with WHP logo is broken or missing.

  • DIRECTIONS

    Adults & Children: Apply locally several times daily or as needed.

  • INACTIVE INGREDIENTS

    34% Ethyl alcohol

    USP water

  • PRINCIPAL DISPLAY PANEL

    WHP Be gone SCRATCH-N-ITCH Label

  • INGREDIENTS AND APPEARANCE
    WHP BE GONE SCRATCH-N-ITCH  TM
    grindelia squarrosa flowering top - camphor (natural) spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68428-983
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GRINDELIA SQUARROSA FLOWERING TOP (UNII: E9Q71VSJ1S) (GRINDELIA SQUARROSA FLOWERING TOP - UNII:E9Q71VSJ1S) GRINDELIA SQUARROSA FLOWERING TOP1 [hp_X]  in 60 mL
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)3 [hp_X]  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68428-983-2760 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/02/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/02/2013
    Labeler - Washington Homeopathic Products (084929389)
    Establishment
    NameAddressID/FEIBusiness Operations
    Washington Homeopathic Products084929389manufacture(68428-983)