Label: CHESTAL COLD AND COUGH- solanum dulcamara top; ferrosoferric phosphate, goldenseal, potassium dichromate, strychnos nux-vomica seed tablet

  • 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 March 20, 2026

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

  • ACTIVE INGREDIENT

    Active ingredients** (in each tablet)

    Dulcamara 5C HPUS (0.5 mg)

    Ferrum phosphoricum 9C HPUS (0.5 mg)

    Hydrastis canadensis 9C HPUS (0.5 mg) (contains less than 10 -19 mg hydrastine and berberine alkaloids)

    Kali bichromicum 9C HPUS (0.5 mg) (contains less than 10 -18 mg chromium)

    Nux vomica 9C HPUS (0.5 mg) (contains less than 10 -19 mg strychnine alkaloids)

    The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

  • PURPOSE

    Purpose*

    Dulcamara 5C HPUS (0.5 mg)…….……………………Relieves colds and coughs worsened by exposure to damp cold

    Ferrum phosphoricum 9C HPUS (0.5 mg)…………….…Relieves colds with gradual onset, occasional minor sore throat, and dry, fitful cough

    Hydrastis canadensis 9C HPUS (0.5 mg)………….Relieves colds and coughs associated with runny nose

    Kali bichromicum 9C HPUS (0.5 mg).……………….………………Relieves nasal discharge

    Nux vomica 9C HPUS (0.5 mg)…….……………………………………..……Relieves sneezing fits

  • INDICATIONS & USAGE

    Uses*

    temporarily relieves symptoms of the common cold such as:

    ▪ nasal and chest congestion ▪ fitful cough ▪ sneezing ▪ occasional minor sore throat
    ▪ runny or stuffy nose

  • WARNINGS

    Do not use if you are allergic to any of this product's ingredients.

  • ASK DOCTOR

    Ask a doctor before use if you have

    ▪ severe sore throat that is accompanied or followed by fever, headache, rash, nausea, or vomiting

    ▪ persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema

    ▪ cough that occurs with too much phlegm (mucus)

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Adults and children 6 years of age and older At the onset of symptoms, dissolve 2 tablets in the mouth every 15 minutes for 1 hour. Then, dissolve 2 tablets in the mouth every 6 hours. Decrease frequency with improvement.

    Children 4 to under 6 years of age Dissolve 2 tablets in 1 tablespoon of water for easier intake. Follow directions above.

    Children under 4 years of age Ask a doctor.

  • INACTIVE INGREDIENT

    croscarmellose sodium, lactose, magnesium stearate

  • QUESTIONS

    1-800-264-7661

  • SPL UNCLASSIFIED SECTION

    ▪ do not use if glued carton end flaps are open or if the blister seal is broken

    ▪ store below 86°F (30°C)

    ▪ retain carton for full drug facts

    COLD & COUGH RELIEF*

    Nasal & Chest Congestion

    Cough • Runny Nose*

    • Day & Night Multi-Symptom Relief
    • Non-Drowsy

    60 MELTAWAY TABLETS

    Unflavored

    Made in France

    Distributed by Boiron Inc.

    Newtown Square, PA 19073

    *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.

    **C, K, CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

  • PRINCIPAL DISPLAY PANEL

    labellabel

  • INGREDIENTS AND APPEARANCE
    CHESTAL COLD AND COUGH 
    solanum dulcamara top; ferrosoferric phosphate, goldenseal, potassium dichromate, strychnos nux-vomica seed tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-9111
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE9 [hp_C]
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED9 [hp_C]
    FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE9 [hp_C]
    SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP5 [hp_C]
    GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL9 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    LACTOSE (UNII: J2B2A4N98G)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUND (Boiron) Size9mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0220-9111-043 in 1 CARTON03/20/2026
    120 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/20/2026
    Labeler - Boiron (282560473)
    Registrant - Boiron, Inc. (014892269)
    Establishment
    NameAddressID/FEIBusiness Operations
    Boiron282560473manufacture(0220-9111)