Label: LUFFA- luffa, hydrastis canadensis, mercurius sulph. rub, allium cepa, natrum muriticum, phosphorus, eupatorium perf, sticta tablet, orally disintegrating

  • NDC Code(s): 60986-2025-2
  • Packager: Marco Pharma International LLC.
  • 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 April 20, 2022

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  • Active Ingredients

    Purging Luffa 6xHPUS

    Goldenseal 4xHPUS

    Cinnabaris 4xHPUS

    Onion 6xHPUS

    Salt 6xHPUS

    Phosphorus 6xHPUS

    Boneset 5xHPUS

    Lungwort 2xHPUS

    The letters HPUS indicates that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of United Sates.

    Purpose

    For relief of sinus symptoms; hay-fever.

    Keep out of reach of children.

    Dosage

    Adults take 1 tablet three times daily, dissolving on the tongue. For severe symptoms, take 1 tablet every hour until improvement is felt. Children receive 1/2 or less the adult amount.

    Warnings

    If pregnant or breast-feeding, consult a health professional before use.

    (Read Suggested Use Section)

    Inactive Ingredients

    In a Lactose base

  • PRINCIPAL DISPLAY PANEL

    Luffa_N10022

  • INGREDIENTS AND APPEARANCE
    LUFFA 
    luffa, hydrastis canadensis, mercurius sulph. rub, allium cepa, natrum muriticum, phosphorus, eupatorium perf, sticta tablet, orally disintegrating
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60986-2025
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LUFFA ACUTANGULA FRUIT (UNII: F0R3Y60C6V) (LUFFA ACUTANGULA FRUIT - UNII:F0R3Y60C6V) LUFFA ACUTANGULA FRUIT6 [hp_X]
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL4 [hp_X]
    MERCURIC SULFIDE (UNII: ZI0T668SF1) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC SULFIDE4 [hp_X]
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION6 [hp_X]
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6 [hp_X]
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS6 [hp_X]
    EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP5 [hp_X]
    LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T) LOBARIA PULMONARIA2 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeCAPSULE (Round Tablet) Size12mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60986-2025-260 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/28/2018
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/01/1992
    Labeler - Marco Pharma International LLC. (161994277)
    Registrant - Marco Pharma International LLC. (161994277)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nestmann Pharma GmbH323426262manufacture(60986-2025)
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