Label: MUCOR- mucor racemosus liquid

  • 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 December 21, 2009

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

  • SPL UNCLASSIFIED SECTION

    Homeopathic Medicine

  • Indications

    For temporary relief of dry, itching, or burning eyes due to allergic or other irritating factors

  • Dosage

    1 drop twice daily, into affected eye(s).

  • Active Ingredient

    Mucor racemosus 5X

  • Inactive Ingredients

    Isotonic sodium chloride solution, chlorhexidine diacetate.

  • Warning

    If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing, seek the advice of a health care professional before using this product.

    Keep this and all medications out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • STORAGE AND HANDLING

    Protect from light and heat.

  • Tamper Evident

    Do not use product if the tamper evident strip is broken or removed from the base of the cap.

  • SPL UNCLASSIFIED SECTION

    To report serious adverse events, call: 1-623-582-3110

    Manufactured for and distributed by:
    USPharmaCo Distribution Ltd.
    2205 W. Lone Cactus Drive #19,
    Phoenix, AZ 85027
    www.uspharmaco.com
    info@uspharmaco.com

    Made in Canada

  • PRINCIPAL DISPLAY PANEL - 5 mL Label

    MUCOR EYE DROPS 5X

    Homeopathic Medicine 0.17 fl. oz. (5ml)

    Indications: For temporary relief of dry, itching, or burning eyes due to allergic or other irriating factors
    Dosage: 1 drop twice daily, into affected eye(s).
    Active Ingredient: Mucor racemosus 5X
    Inactive Ingredients: Isotonic sodium chloride solution, chlorhexidine diacetate.
    Warning: If symptoms persist more than a few days, contact a licensed practitioner. As with any
    drug, if you are pregnant or nursing, seek the advice of a health care professional before using this
    product. Keep this and all medications out of reach of children. In case of overdose, get medical help
    or contact a Poison Control Center right away. Protect from light and heat.
    Tamper Evident: Do not use product if the tamper evident strip is broken or removed from the base
    of the cap.
    To report serious adverse events, call: 1-623-582-3110

    Principal Display Panel - 5 mL Label
  • INGREDIENTS AND APPEARANCE
    MUCOR 
    mucor racemosus liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49693-1306
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Mucor racemosus (UNII: 17RH99LQ7G) (Mucor racemosus - UNII:17RH99LQ7G) Mucor racemosus5 [hp_X]  in 5 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49693-1306-11 in 1 BOX
    15 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC12/15/2009
    Labeler - USPharmaCo (145322622)
    Establishment
    NameAddressID/FEIBusiness Operations
    DermaMed256799461MANUFACTURE