Label: BERBERIS ANTISEPTIC- berberis aquifolium, calendula officinalis, hydrastis canadensis, acid boric, zinc oxide, borax, calcium sulphate, antimonium crudum cream

  • 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 November 10, 2010

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  • ACTIVE INGREDIENT


    Berberis Aq. - 0.1ml
    Calendula - 0.1ml
    Hydrastis Can. - 0.1ml
    Acid Boric - 1x 10mg
    Zinc Oxide - 1x 5mg
    Borax - 1x5mg
    Calc. Sulph. - 1x 2mg
    Ant. Crude - 1x 2mg
  • INACTIVE INGREDIENT

    Alcohol - 4.8 percent v/v

  • PURPOSE

    Berberis is a flowered shrub known to aid in the care of acne, blemishes, and the smoothing of complexion. The unique combination of Berberis Antiseptic Cream helps to cleanse pores and leaves your skin feeling silky smooth.

  • INDICATIONS & USAGE

    Berberis. A natural solution for acne and blemishes.

    - Cleanses Pores

    -Clears Complexion

  • DOSAGE & ADMINISTRATION

    Apply and rub onto skin as needed.

  • WARNINGS

    - For external use only.

    - Store in a cool, dry place.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • HOW SUPPLIED

    Berberis Antiseptic Cream is manufactured in India with the highest quality ingredients for Regranion, LLC, Charleston, SC 29403

  • REFERENCES

    Questions? Comments?
    Call 1-877-648-8443

  • PRINCIPAL DISPLAY PANEL


    Berberis Full Label

  • INGREDIENTS AND APPEARANCE
    BERBERIS  ANTISEPTIC
    berberis aquifolium, calendula officinalis, hydrastis canadensis, acid boric, zinc oxide, borax, calcium sulphate, antimonium crudum cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51720-421
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (MAHONIA AQUIFOLIUM ROOT BARK - UNII:VZJ9F3C3SB) MAHONIA AQUIFOLIUM ROOT BARK 2 [hp_X]  in 21 g
    CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP2 [hp_X]  in 21 g
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL2 [hp_X]  in 21 g
    BORIC ACID (UNII: R57ZHV85D4) (BORIC ACID - UNII:R57ZHV85D4) BORIC ACID1 [hp_X]  in 21 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE1 [hp_X]  in 21 g
    SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22) SODIUM BORATE1 [hp_X]  in 21 g
    CALCIUM SULFATE (UNII: WAT0DDB505) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE1 [hp_X]  in 21 g
    ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY - UNII:9IT35J3UV3) ANTIMONY TRISULFIDE1 [hp_X]  in 21 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M) 1 mL  in 21 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51720-421-581 in 1 BOX
    1NDC:51720-421-5621 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/15/2009
    Labeler - Curative Power Lab PVT LTD (650500981)
    Registrant - Curative Power Lab PVT LTD (650500981)
    Establishment
    NameAddressID/FEIBusiness Operations
    Curative Power Lab PVT LTD650500981manufacture
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