Label: GINSENG DROPS- panax ginseng solution

  • NDC Code(s): 82797-221-30
  • Packager: Dr. Masood Homeopathic Pharmaceuticals Private Limited
  • 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 May 9, 2024

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  • DOSAGE & ADMINISTRATION

    Dosage and Adminstration

    5-10 drops three times a day.

  • INACTIVE INGREDIENT

    Inactive Ingredient:

    Ethyl Alcohil 90%

  • ACTIVE INGREDIENT

    Active Ingredients:

    Panax quinquefolium (American Ginseng) 1% v/v

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children:

    Keep this and all medicnes out of the reach of children

  • INDICATIONS & USAGE

    Indications and Usage :

    A homeopathic remedy for health and longevity. strengthens nervous sytem, digestion an dmental faculties,

    Recommended for old age complaints, exhaustion, backache, rheumatism, headache, cough, indigestion, irritability and anxiety

  • PURPOSE

    Purpose:

    Helps boost Immunity, Stamina, Strength and Performance

    Combats Stress and Anxiety

  • WARNINGS

    Warnings:

    Do not:

    • use if you have an allergy or hypersensitivity to components of the formula
    • apply to wound or damaged skin
    • use if pregnant or nursing

    Stop use and ask a doctor if:

    • condition worsens
    • If symptoms persists for more than 7 days

  • PRINCIPAL DISPLAY PANEL

    Ginseng drops

  • INGREDIENTS AND APPEARANCE
    GINSENG DROPS 
    panax ginseng solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82797-221
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PANAX QUINQUEFOLIUS WHOLE (UNII: 0P067WOA1X) (PANAX QUINQUEFOLIUS WHOLE - UNII:0P067WOA1X) PANAX QUINQUEFOLIUS WHOLE1 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M) 29.7 mL  in 30 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82797-221-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product05/09/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/09/2024
    Labeler - Dr. Masood Homeopathic Pharmaceuticals Private Limited (645453119)
    Registrant - Dr. Masood Homeopathic Pharmaceuticals Private Limited (645453119)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dr. Masood Homeopathic Pharmaceuticals Private Limited645453119manufacture(82797-221) , pack(82797-221) , label(82797-221)
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