Label: UNDA 25- argentum metallicum, crataegus, gelsemium sempervirens, hamamelis virginiana, magnolia grandiflora, spiraea ulmaria, stannum metallicum, valeriana officinalis liquid
UNDA 27- antimonium crudum, borago officinalis, cetraria islandica, drosera, mentha piperita, senega officinalis liquid
UNDA 22- absinthium, aconitum napellus, argentum metallicum, boldo leaf, chamomilla, coffea tosta, jateorhiza palmata, manganum oxydatum nigrum, salvia officinalis liquid
UNDA 12- argentum metallicum, aurum metallicum, dulcamara, fagopyrum esculentum, illicium verum, lappa major, salvia officinalis, sarsaparilla, staphysagria, viola tricolor liquid

  • NDC Code(s): 62106-1121-8, 62106-1124-8, 62106-1126-8, 62106-1152-8
  • Packager: Seroyal USA
  • Category: HUMAN OTC DRUG LABEL

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 July 15, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:

    Argentum metallicum (Silver) 12X
    Aurum metallicum (Gold) 12X
    Dulcamara (Bittersweet) Shoots 4X
    Fagopyrum esculentum Aerial Parts 4X
    Illicium verum (Star Anise) Fruit 4X
    Lappa major (Great burdock) Root 4X
    Salvia officinalis (Garden sage) Leaf 4X
    Sarsaparilla Root 4X
    Staphysagria (Stavesacre) Seed 12X
    Viola tricolor (Pansy) Aerial Parts 4X

  • PURPOSE

    Uses

    For the temporary relief of symptoms associated with mild skin irritation.

  • 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 mild skin irritation.

    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:

    Absinthium (Common wormwood) Aerial Parts 4X
    Aconitum napellus (Aconite) Whole Plant 4X
    Argentum metallicum (Silver) 12X
    Boldo Leaf 4X
    Chamomilla (German chamomile) Whole Flowering Plant 4X
    Coffea tosta (Roasted coffee) Seed 4X
    Jateorhiza palmata (Columbo) Root 4X
    Manganum oxydatum nigrum (Manganese dioxide) 12X
    Salvia officinalis (Garden sage) Leaf 4X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with mild anxiousness 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.

    Contents may not fill package in order
    to accommodate required labeling.
    Please rely on stated quantity.

  • 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 mild anxiousness 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:
    Argentum metallicum (Silver) 12X
    Crataegus (Hawthorn) Fruit 4X
    Gelsemium sempervirens (Yellow jessamine) Underground Parts 4X
    Hamamelis virginiana (Witch hazel) Bark 4X
    Magnolia grandiflora Flower 4X
    Spiraea ulmaria (Queen-of-the-meadow) Underground Parts 4X
    Stannum metallicum (Tin) 12X
    Valeriana officinalis (Valerian) Root 4X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with
    coldness or numbness of the extremities.

  • 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

  • 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
    coldness or numbness of the extremities.

    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.

  • OTHER SAFETY INFORMATION

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

  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:
    Antimonium crudum (Antimonous sulfide) 12X
    Borago officinalis (Common borage) Leaf 4X
    Cetraria islandica (Iceland moss) Whole Plant 4X
    Drosera (Sundew) Whole Plant 4X
    Mentha piperita (Peppermint) Aerial Parts 4X
    Senega officinalis (Snakeroot) Root 4X

  • PURPOSE

    Uses
    For the relief of symptoms associated with laryngitis and voice hoarseness.

  • WARNINGS

    Warnings

    Ask a doctor before use if you have Persistent cough or chronic cough
    such as occurs with smoking, asthma, chronic bronchitis, or emphysema and Cough that is accompanied by
    excessive phlegm (mucus) or fever.

    Stop use and ask a doctor if symptoms persist or worsen and Cough persists for more than 1 week,
    tends to recur, or is accompanied by a fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.
    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 and Cough persists for more than 1 week,

    tends to recur, or is accompanied by a fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.

  • 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.

  • ASK DOCTOR

    Ask a doctor before use if you have Persistent cough or chronic cough
    such as occurs with smoking, asthma, chronic bronchitis, or emphysema and Cough that is accompanied by
    excessive phlegm (mucus) or fever.

  • 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 relief of symptoms associated with laryngitis and voice hoarseness.

    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

    62106-1152

    NDC 62106-1152-8

    UNDA

    numbered compounds

    UNDA 12

    Homeopathic Preparation

    For the temporary relief of symptoms

    associated with mild skin irritation.

    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1121-8

    NDC 62106-1121-8

    UNDA
    numbered compounds
    UNDA 22
    Homeopathic Preparation

    For the temporary relief of symptoms
    associated with mild anxiousness
    and nervousness.
    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1124

    NDC 62106-1124-8

    UNDA
    numbered compounds
    UNDA 25
    Homeopathic Preparation

    For the temporary relief of symptoms
    associated with coldness or numbness
    of the extremities.
    Contains 31% Alcohol
    0.7 fl oz (20 ml)

  • PRINCIPAL DISPLAY PANEL

    62106-1126

    UNDA
    NDC 62106-1126-8
    numbered compounds
    UNDA 27
    Homeopathic Preparation

    For the relief of symptoms associated with laryngitis and voice hoarseness.
    Contains 31% Alcohol
    0.7 fl oz (20 mL)

  • INGREDIENTS AND APPEARANCE
    UNDA 25 
    argentum metallicum, crataegus, gelsemium sempervirens, hamamelis virginiana, magnolia grandiflora, spiraea ulmaria, stannum metallicum, valeriana officinalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1124
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER12 [hp_X]  in 20 mL
    FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (FILIPENDULA ULMARIA ROOT - UNII:997724QNDS) FILIPENDULA ULMARIA ROOT4 [hp_X]  in 20 mL
    CRATAEGUS FRUIT (UNII: Q21UUL2105) (CRATAEGUS FRUIT - UNII:Q21UUL2105) CRATAEGUS FRUIT4 [hp_X]  in 20 mL
    TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN12 [hp_X]  in 20 mL
    VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN4 [hp_X]  in 20 mL
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT4 [hp_X]  in 20 mL
    HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (HAMAMELIS VIRGINIANA BARK - UNII:IH3063S9MY) HAMAMELIS VIRGINIANA BARK4 [hp_X]  in 20 mL
    MAGNOLIA GRANDIFLORA FLOWER (UNII: RV23PE6426) (MAGNOLIA GRANDIFLORA FLOWER - UNII:RV23PE6426) MAGNOLIA GRANDIFLORA FLOWER4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1124-81 in 1 CARTON09/21/2015
    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 homeopathic09/21/2015
    UNDA 27 
    antimonium crudum, borago officinalis, cetraria islandica, drosera, mentha piperita, senega officinalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1126
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U) ANTIMONY TRISULFIDE12 [hp_X]  in 20 mL
    BORAGE (UNII: PB618V0K2W) (BORAGE - UNII:PB618V0K2W) BORAGE4 [hp_X]  in 20 mL
    CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (CETRARIA ISLANDICA SUBSP. ISLANDICA - UNII:BJ7YPN79A1) CETRARIA ISLANDICA SUBSP. ISLANDICA4 [hp_X]  in 20 mL
    DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG) DROSERA ROTUNDIFOLIA FLOWERING TOP4 [hp_X]  in 20 mL
    MENTHA PIPERITA (UNII: 79M2M2UDA9) (MENTHA PIPERITA - UNII:79M2M2UDA9) MENTHA PIPERITA4 [hp_X]  in 20 mL
    POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF) POLYGALA SENEGA ROOT4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1126-81 in 1 CARTON09/21/2015
    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 homeopathic09/21/2015
    UNDA 22 
    absinthium, aconitum napellus, argentum metallicum, boldo leaf, chamomilla, coffea tosta, jateorhiza palmata, manganum oxydatum nigrum, salvia officinalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1121
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MANGANESE DIOXIDE (UNII: TF219GU161) (MANGANESE DIOXIDE - UNII:TF219GU161) MANGANESE DIOXIDE12 [hp_X]  in 20 mL
    SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE4 [hp_X]  in 20 mL
    PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) (PEUMUS BOLDUS LEAF - UNII:Q4EWM09M3O) PEUMUS BOLDUS LEAF4 [hp_X]  in 20 mL
    MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ) MATRICARIA RECUTITA4 [hp_X]  in 20 mL
    JATEORHIZA CALUMBA ROOT (UNII: V36I2B8LD5) (JATEORHIZA CALUMBA ROOT - UNII:V36I2B8LD5) JATEORHIZA CALUMBA ROOT4 [hp_X]  in 20 mL
    WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD4 [hp_X]  in 20 mL
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS4 [hp_X]  in 20 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER12 [hp_X]  in 20 mL
    COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (COFFEA ARABICA SEED, ROASTED - UNII:9H58JRT35E) COFFEA ARABICA SEED, ROASTED4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1121-81 in 1 CARTON09/21/2015
    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 homeopathic09/21/2015
    UNDA 12 
    argentum metallicum, aurum metallicum, dulcamara, fagopyrum esculentum, illicium verum, lappa major, salvia officinalis, sarsaparilla, staphysagria, viola tricolor liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1152
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GOLD (UNII: 79Y1949PYO) (GOLD - UNII:79Y1949PYO) GOLD12 [hp_X]  in 20 mL
    SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP4 [hp_X]  in 20 mL
    FAGOPYRUM ESCULENTUM (UNII: B10M69172N) (FAGOPYRUM ESCULENTUM - UNII:B10M69172N) FAGOPYRUM ESCULENTUM4 [hp_X]  in 20 mL
    STAR ANISE FRUIT (UNII: CK15HA8438) (STAR ANISE FRUIT - UNII:CK15HA8438) STAR ANISE FRUIT4 [hp_X]  in 20 mL
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) (ARCTIUM LAPPA ROOT - UNII:597E9BI3Z3) ARCTIUM LAPPA ROOT4 [hp_X]  in 20 mL
    SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE4 [hp_X]  in 20 mL
    SARSAPARILLA (UNII: 2H1576D5WG) (SARSAPARILLA - UNII:2H1576D5WG) SARSAPARILLA4 [hp_X]  in 20 mL
    DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (DELPHINIUM STAPHISAGRIA SEED - UNII:00543AP1JV) DELPHINIUM STAPHISAGRIA SEED12 [hp_X]  in 20 mL
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER12 [hp_X]  in 20 mL
    VIOLA TRICOLOR (UNII: 9Q24RAI43V) (VIOLA TRICOLOR - UNII:9Q24RAI43V) VIOLA TRICOLOR4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1152-81 in 1 CARTON09/21/2015
    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 homeopathic09/21/2015
    Labeler - Seroyal USA (018361118)
    Establishment
    NameAddressID/FEIBusiness Operations
    SAN’UP401010287manufacture(62106-1152, 62106-1121, 62106-1124, 62106-1126)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!