Label: UNDA 220- grindelia, pilocarpus, salvia officinalis, senega officinalis, stramonium, valeriana officinalis liquid
UNDA 273- arnica montana, equisetum arvense, polygonum hydropiperoides, rubus fruticosus, verbascum densiflorum liquid

  • NDC Code(s): 62106-1157-8, 62106-1167-8
  • 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 November 9, 2022

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

  • ACTIVE INGREDIENT

    Active ingredients

    Each drop contains:

    Grindelia Aerial Parts 6X
    Pilocarpus Leaf 6X
    Salvia officinalis (Garden sage) Leaf 6X
    Senega officinalis Root 6X
    Stramonium (Thorn apple) Aerial Parts 6X
    Valeriana officinalis (Valerian) Root 6X

  • PURPOSE

    Uses
    For the temporary relief of symptoms associated with cough.

  • WARNINGS

    Warnings
    Ask a doctor before use if you have

    Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.

    Cough that is accompanied by excessive phlegm (mucus) or fever.

    Stop use and ask a doctor if
    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.
    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
    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.
    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 cough.

    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:

    Arnica montana (Mountain Arnica) Root 4X
    Equisetum arvense (Common Horsetail) Stem 4X
    Polygonum hydropiperoides (Mild water pepper) Whole Plant 4X
    Rubus fruticosus (Shrubby blackberry) Leaf 4X
    Verbascum densiflorum Aerial Parts 4X

  • PURPOSE

    Uses

    For the temporary relief of symptoms associated with 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

    Uses

    For the temporary relief of symptoms associated with 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.

  • PRINCIPAL DISPLAY PANEL

    62106-1157-8

    NDC 62106-1157-8

    UNDA
    numbered compounds
    UNDA 220
    Homeopathic Preparation

    For the temporary
    relief of symptoms
    associated with cough.
    Contains 31% Alcohol
    0.7 fl oz (20 mL)

  • PRINCIPAL DISPLAY PANEL

    62106-1167-8

    NDC 62106-1167-8

    UNDA
    numbered compounds
    UNDA 273
    Homeopathic Preparation

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

  • INGREDIENTS AND APPEARANCE
    UNDA 220 
    grindelia, pilocarpus, salvia officinalis, senega officinalis, stramonium, valeriana officinalis liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1157
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GRINDELIA HIRSUTULA FLOWERING TOP (UNII: IDB0NAZ6AI) (GRINDELIA HIRSUTULA FLOWERING TOP - UNII:IDB0NAZ6AI) GRINDELIA HIRSUTULA FLOWERING TOP6 [hp_X]  in 20 mL
    PILOCARPUS MICROPHYLLUS LEAF (UNII: TY68V0X4KL) (PILOCARPUS MICROPHYLLUS LEAF - UNII:TY68V0X4KL) PILOCARPUS MICROPHYLLUS LEAF6 [hp_X]  in 20 mL
    SAGE (UNII: 065C5D077J) (SAGE - UNII:065C5D077J) SAGE6 [hp_X]  in 20 mL
    DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3) DATURA STRAMONIUM6 [hp_X]  in 20 mL
    VALERIAN (UNII: JWF5YAW3QW) (VALERIAN - UNII:JWF5YAW3QW) VALERIAN6 [hp_X]  in 20 mL
    POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (POLYGALA SENEGA ROOT - UNII:M7T6H7D4IF) POLYGALA SENEGA ROOT6 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1157-81 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 273 
    arnica montana, equisetum arvense, polygonum hydropiperoides, rubus fruticosus, verbascum densiflorum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62106-1167
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARNICA MONTANA ROOT (UNII: MUE8Y11327) (ARNICA MONTANA ROOT - UNII:MUE8Y11327) ARNICA MONTANA ROOT4 [hp_X]  in 20 mL
    EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E) (EQUISETUM ARVENSE BRANCH - UNII:1L0VKZ185E) EQUISETUM ARVENSE BRANCH4 [hp_X]  in 20 mL
    PERSICARIA PUNCTATA (UNII: D32E7AXD4R) (PERSICARIA PUNCTATA - UNII:D32E7AXD4R) PERSICARIA PUNCTATA4 [hp_X]  in 20 mL
    RUBUS FRUTICOSUS LEAF (UNII: YQ2S06L8S9) (RUBUS FRUTICOSUS LEAF - UNII:YQ2S06L8S9) RUBUS FRUTICOSUS LEAF4 [hp_X]  in 20 mL
    VERBASCUM DENSIFLORUM FLOWERING TOP (UNII: 8LR978PU7Y) (VERBASCUM DENSIFLORUM FLOWERING TOP - UNII:8LR978PU7Y) VERBASCUM DENSIFLORUM FLOWERING TOP4 [hp_X]  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62106-1167-81 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
    SAN’UP401010287manufacture(62106-1157, 62106-1167)