Label: UNDA 43- aluminium metallicum, asperula odorata, equisetum arvense, jateorhiza palmata, marrubium vulgare, ocimum basilicum, stannum metallicum liquid
UNDA 47- absinthium, arnica montana, aurum metallicum, jateorhiza palmata, rosmarinus officinalis, stibium metallicum, thymus vulgaris, valeriana officinalis liquid

  • NDC Code(s): 62106-1142-8, 62106-1146-8
  • Packager: Seroyal USA
  • 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 October 4, 2017

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

  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:

    Absinthium (Common wormwood) Aerial Parts 6X
    Arnica montana (Mountain arnica) Underground Parts 6X
    Aurum metallicum (Gold) 12X
    Jateorhiza palmata (Columbo) Root 6X
    Rosmarinus officinalis (Rosemary) Leaf 6X
    Stibium metallicum (Antimony) 15X
    Thymus vulgaris Aerial Parts 6X
    Valeriana officinalis (Valerian) Root 6X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with dizziness, mental fatigue and nervousness.

  • WARNINGS

    Warnings
    Stop use and ask a doctor if symptoms persist or worsen.
    If pregnant or breastfeeding, 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.

  • STOP USE

    Stop use and ask a doctor if symptoms persist or worsen.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    Inactive ingredients
    Ethanol (beet), purified water

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.

  • DOSAGE & ADMINISTRATION

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • INDICATIONS & USAGE

    UsesUses
    For the temporary relief of symptoms associated with dizziness, mental fatigue and nervousness.

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:

    Aluminium metallicum (Aluminum) 12X
    Asperula odorata (Sweet woodruff) Aerial Parts 4X
    Equisetum arvense (Common horsetail) Stem 4X
    Jateorhiza palmata (Columbo) Root 4X
    Marrubium vulgare (Common horehound) Aerial Parts 4X
    Ocimum basilicum Aerial Parts 4X
    Stannum metallicum (Tin) 12X

  • PURPOSE

    Uses

    For the temporary relief of symptoms associated with poor digestion.

  • WARNINGS

    Warnings
    Stop use and ask a doctor if symptoms persist or worsen.
    If pregnant or breastfeeding, 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.

  • STOP USE

    Stop use and ask a doctor if symptoms persist or worsen.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    Inactive ingredients
    Ethanol (beet), purified water

  • OTHER SAFETY INFORMATION

    Other information
    Do not use if seal is missing or broken.
    Store in a cool, dry place.

  • DOSAGE & ADMINISTRATION

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • INDICATIONS & USAGE

    Uses

    For the temporary relief of symptoms associated with poor digestion.

    Directions
    Adults and adolescents (12 years and older): Take 5 drops three times daily or as
    recommended by your healthcare practitioner.
    Children (under 12 years): Take under the direction of your
    healthcare practitioner.

  • PRINCIPAL DISPLAY PANEL

    62106-1146

    NDC 62106-1146-8

    UNDA

    numbered compounds
    UNDA 47
    Homeopathic Preparation

    For the temporary relief of symptoms
    associated with dizziness, mental
    fatigue and nervousness.
    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1142

    NDC 62106-1142-8

    UNDA
    numbered compounds
    UNDA 43
    Homeopathic Preparation

    For the temporary relief of symptoms
    associated with poor digestion.
    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • INGREDIENTS AND APPEARANCE
    UNDA 43 
    aluminium metallicum, asperula odorata, equisetum arvense, jateorhiza palmata, marrubium vulgare, ocimum basilicum, stannum metallicum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1142
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z) (EQUISETUM ARVENSE TOP - UNII:1DP6Y6B65Z) EQUISETUM ARVENSE TOP4 [hp_X]  in 20 mL
    JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (JATEORHIZA CALUMBA ROOT - UNII:V36I2B8LD5) JATEORHIZA CALUMBA ROOT4 [hp_X]  in 20 mL
    GALIUM ODORATUM (UNII: N8C4A9A49H) (GALIUM ODORATUM - UNII:N8C4A9A49H) GALIUM ODORATUM4 [hp_X]  in 20 mL
    MARRUBIUM VULGARE (UNII: 7A72MUN24Z) (MARRUBIUM VULGARE - UNII:7A72MUN24Z) MARRUBIUM VULGARE4 [hp_X]  in 20 mL
    BASIL (UNII: 2U0KZP0FDW) (BASIL - UNII:2U0KZP0FDW) BASIL4 [hp_X]  in 20 mL
    TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN12 [hp_X]  in 20 mL
    ALUMINUM (UNII: CPD4NFA903) (ALUMINUM - UNII:CPD4NFA903) ALUMINUM12 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1142-81 in 1 CARTON09/22/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/22/2015
    UNDA 47 
    absinthium, arnica montana, aurum metallicum, jateorhiza palmata, rosmarinus officinalis, stibium metallicum, thymus vulgaris, valeriana officinalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1146
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II) (THYMUS VULGARIS WHOLE - UNII:8L72OKJ7II) THYMUS VULGARIS WHOLE6 [hp_X]  in 20 mL
    VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN6 [hp_X]  in 20 mL
    WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD6 [hp_X]  in 20 mL
    ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT6 [hp_X]  in 20 mL
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD12 [hp_X]  in 20 mL
    JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (JATEORHIZA CALUMBA ROOT - UNII:V36I2B8LD5) JATEORHIZA CALUMBA ROOT6 [hp_X]  in 20 mL
    ROSEMARY (UNII: IJ67X351P9) (ROSEMARY - UNII:IJ67X351P9) ROSEMARY6 [hp_X]  in 20 mL
    ANTIMONY (UNII: 9IT35J3UV3) (ANTIMONY - UNII:9IT35J3UV3) ANTIMONY15 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1146-81 in 1 CARTON09/22/2015
    120 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/22/2015
    Labeler - Seroyal USA (018361118)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unda SA400346069manufacture(62106-1142, 62106-1146)