Label: DR. TALBOTS MUCUS COLD RELIEF- eupatorium perf, hepar sulphuris calcareum, kali bichromicum, marrubium vulgare, phosphorus, pulsatilla, rumex crispus, sambucus nigra, calcarea sulphurica, ferrum phosphoricum, kali muriaticum liquid

  • NDC Code(s): 70797-313-01, 70797-313-04
  • 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
    Eupatorium perf 12X HPUS
    Hepar sulphuris calcareum 12X HPUS
    Kali bichromicum 12X HPUS
    Marrubium vulgare 12X HPUS
    Phosphorus 30X HPUS
    Pulsatilla 12X HPUS
    Rumex crispus 12X HPUS
    Sambucus nigra 12x HPUS
    Cell Salts
    Calcarea sulphurica 12X HPUS
    Ferrum phosphoricum 12X HPUS
    Kali muriaticum 6X HPUS

    Active Ingredients

  • Purpose

    Purpose
    Congestion, soreness
    Yellowish mucus discharge

    Sinus congestion
    Cough with expectoration
    Chest congestion
    Discharge of thick yellowish mucus
    Copious mucus discharge
    Nasal congestion
    Thick mucus yellowish discharges
    Congestion and inflammation of mucus membranes
    Inflammation with discharge

    Purpose

  • Uses

    Uses

    Temporarily relieves

    • mucusy cough
    • cough and congestion associated with colds
    • nasal and sinus congestion
    • mucus in chest
    • sneezing
    • runny nose

    Indication

  • 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/congestion lasts for more than 7 days.
    • cough/congestion comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious confition.
    • other symptoms persist for more than 7 days or worsen
    • 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.

    Warning

  • Pregnancy or breastfeeding

    If pregnant or breastfeeding, consult your doctor before use.

    Pregnancy

  • 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.

    Keep out of reach of children

  • 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

    Dosage

  • Inactive Ingredients

    Inactive Ingredients

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

    Inactive ingredient

  • Questions

    Questions or Comments?

    Call us at 1-800-588-6227

    M-F 8am-5pm CST

    Questions

  • Principal Display Panel

    PDP

  • INGREDIENTS AND APPEARANCE
    DR. TALBOTS MUCUS COLD RELIEF 
    eupatorium perf, hepar sulphuris calcareum, kali bichromicum, marrubium vulgare, phosphorus, pulsatilla, rumex crispus, sambucus nigra, calcarea sulphurica, ferrum phosphoricum, kali muriaticum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70797-313
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (EUPATORIUM PERFOLIATUM FLOWERING TOP - UNII:1W0775VX6E) EUPATORIUM PERFOLIATUM FLOWERING TOP12 [hp_X]  in 118 mL
    SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (SAMBUCUS NIGRA FLOWERING TOP - UNII:CT03BSA18U) SAMBUCUS NIGRA FLOWERING TOP12 [hp_X]  in 118 mL
    CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM SULFATE ANHYDROUS12 [hp_X]  in 118 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE6 [hp_X]  in 118 mL
    MARRUBIUM VULGARE (UNII: 7A72MUN24Z) (MARRUBIUM VULGARE - UNII:7A72MUN24Z) MARRUBIUM VULGARE12 [hp_X]  in 118 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS30 [hp_X]  in 118 mL
    RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (RUMEX CRISPUS ROOT - UNII:9N1RM2S62C) RUMEX CRISPUS ROOT12 [hp_X]  in 118 mL
    FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE12 [hp_X]  in 118 mL
    CALCIUM SULFIDE (UNII: 1MBW07J51Q) (CALCIUM SULFIDE - UNII:1MBW07J51Q) CALCIUM SULFIDE12 [hp_X]  in 118 mL
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE12 [hp_X]  in 118 mL
    ANEMONE PULSATILLA (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) ANEMONE PULSATILLA12 [hp_X]  in 118 mL
    Inactive Ingredients
    Ingredient NameStrength
    CONCORD GRAPE JUICE (UNII: F7039Q79LP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70797-313-011 in 1 CARTON07/20/2020
    1NDC:70797-313-04118 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)