Label: GUNA-RERIO- danio rerio egg solution/ drops

  • 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, 2018

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  • ACTIVE INGREDIENTS/PURPOSE

    Rerio fish extract    4x    Antioxidant

  • USES

    Temporary relief of symptoms due to debilitating illness such as:

    • Weakness
    • Malaise
    • Loss of endurance
  • WARNINGS

    Stop use and ask doctor if symptoms persist more than 5 days.
    If pregnant or breast-feeding ask a health professional before use.
    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
    Contains ethyl alcohol 30%

  • PREGNANCY

    If pregnant or breast-feeding ask a doctor before use

  • WARNINGS

    Keep out of reach of children

  • DIRECTIONS

    Take 15 minutes before meals

    Adults and children 12 years and older 20 drops in a little water, 2 times per day

    Children between 12 years and 6 years of age 10 drops in a little water, 2 times per day

    Children under 6 years 5 drops in a glass of water, 2 times per day

  • QUESTIONS

    Questions?: info@gunainc.com, tel. (484) 223-3500

  • INDICATIONS & USAGE

    Take 15 minutes before meals

  • INACTIVE INGREDIENT

    Inactive ingredient: Ethyl alcohol 30%.

  • PRINCIPAL DISPLAY PANEL

    5USGRE-Guna-Rerio rev03-100718

  • INGREDIENTS AND APPEARANCE
    GUNA-RERIO 
    danio rerio egg solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17089-337
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DANIO RERIO EGG (UNII: S6FVH88J8W) (DANIO RERIO EGG - UNII:S6FVH88J8W) DANIO RERIO EGG4 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M) 9 mL  in 30 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17089-337-181 in 1 BOX12/21/2018
    130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/18/2007
    Labeler - Guna spa (430538264)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guna spa338587646manufacture(17089-337)
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