Label: DR. TALBOTS COUGH RELIEF- antimonium tartaricum, drosera rotundifolia, ipecacuanha, phosphorus, rumex crispus, spongia tosta, sticta pulmonaria, kali sulphuricum liquid

  • NDC Code(s): 70797-314-01, 70797-314-04
  • Packager: Talbot's Pharmaceuticals Family Products, 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 October 5, 2021

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

  • Active Ingredients

    Active Ingredients
    Antimonium tartaricum 12X HPUS
    Drosera rotundifolia 12X HPUS
    Ipecacuanha 12X HPUS
    Phosphorus 12X HPUS
    Rumex crispus 12X HPUS
    Spongia Tosta 12X HPUS
    Sticta pulmonaria 12X HPUS
    Cell Salts
    Kali sulphuricum 6X HPUS

  • Uses

    Uses

    Temporarily relieves

    • sore throat
    • dry, tickling, mucusy, and/or spasmodic coughs associated with colds
    • chest congestion

  • Warnings

    Do not use:

    • for persistent or chronic cough
    • for treating cough from asthma, smoking, or emphysema
    • for treating cough with excessive mucus

    A persistent cough may be a sign of a serious condition

    Stop use and ask doctor if:

    • cough lasts for more than 7 days
    • cough comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
    • Ask a doctor before use if you are taking a prescription drug or have a serious medical condition.
    • Please consult your physician immediately for a worsening condition.

  • Pregnancy or breastfeeding

    If pregnant or breastfeeding, consult your doctor before use.

  • Keep out of reach of children

    Keep out of reach of children. In case of overdoes (or accidental ingestion), get medical help or contact a Poison Control Center right away. DO NOT USE IF SEAL UNDER CAP IS BROKEN OR MISSING.

  • Directions

    • Shake before use, natural juice may settle
    • Measure only with the dosing syringe provided
    • Do not use dosing syringe with other products
    • On dosing syringe, weight is specific to product
    • On dosing syringe, ml = milliliter, lbs = pounds, kgs = kilograms

    Children under 6 months of age, consult a medical professional before using this product.

    For sudden onset of symptoms: Use every 15 minutes for up to 8 doses until symptoms relieved, then every 2 hours thereafter.

    Children 6 - 18 lbs or 3 - 8 kgs

    1.25 ml every 2 hours, reduce frequency when symptoms improve

    Children 19 - 29 lbs or 9 - 13 kgs

    2.5 ml every 2 hours, reduce frequency when symptoms improve

    Children 30 - 90 lbs or 14 - 41 kgs

    5 ml every 2 hours, reduce frequency when symptoms improve

  • Inactive Ingredients

    Inactive ingredients

    Citric acid, elderberry juice, glycerin, grape juice, potassium sorbate, purified water

  • Questions

    Questions or Comments?

    Call us at 1-800-588-6227

    M-F 8am-5pm CST

  • Purpose

    Purpose
    Thick mucus
    Spasmodic cough
    Gagging cough
    Oppresive cough
    Barking cough
    Dry cough
    Hacking cough
    Rattling of mucus in chest

  • Principal Display Panel

    PDP

  • INGREDIENTS AND APPEARANCE
    DR. TALBOTS COUGH RELIEF 
    antimonium tartaricum, drosera rotundifolia, ipecacuanha, phosphorus, rumex crispus, spongia tosta, sticta pulmonaria, kali sulphuricum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70797-314
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PULMONARIA OFFICINALIS WHOLE (UNII: 483B0A2Y00) (PULMONARIA OFFICINALIS WHOLE - UNII:483B0A2Y00) PULMONARIA OFFICINALIS WHOLE12 [hp_X]  in 118 mL
    ANTIMONY TARTRATE ION (UNII: CQN5KB2U1M) (ANTIMONY TARTRATE ION - UNII:CQN5KB2U1M) ANTIMONY TARTRATE ION12 [hp_X]  in 118 mL
    DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (DROSERA ROTUNDIFOLIA FLOWERING TOP - UNII:75O014T1HG) DROSERA ROTUNDIFOLIA FLOWERING TOP12 [hp_X]  in 118 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS12 [hp_X]  in 118 mL
    RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT12 [hp_X]  in 118 mL
    POTASSIUM SULFATE (UNII: 1K573LC5TV) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM SULFATE6 [hp_X]  in 118 mL
    SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (SPONGIA OFFICINALIS SKELETON, ROASTED - UNII:1PIP394IID) SPONGIA OFFICINALIS SKELETON, ROASTED12 [hp_X]  in 118 mL
    IPECAC (UNII: 62I3C8233L) (IPECAC - UNII:62I3C8233L) IPECAC12 [hp_X]  in 118 mL
    Inactive Ingredients
    Ingredient NameStrength
    EUROPEAN ELDERBERRY JUICE (UNII: Z4IFJ0AK1E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    CONCORD GRAPE JUICE (UNII: F7039Q79LP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70797-314-011 in 1 CARTON07/20/2020
    1NDC:70797-314-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/20/2020
    Labeler - Talbot's Pharmaceuticals Family Products, LLC. (078855555)