Label: CHESTAL COLD AND COUGH- solanum dulcamara top; ferrosoferric phosphate, goldenseal, potassium dichromate, strychnos nux-vomica seed tablet
- NDC Code(s): 0220-9111-04
- Packager: Boiron
- 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.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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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.
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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
- WARNINGS
- ASK DOCTOR
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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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
- QUESTIONS
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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
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INGREDIENTS AND APPEARANCE
CHESTAL COLD AND COUGH
solanum dulcamara top; ferrosoferric phosphate, goldenseal, potassium dichromate, strychnos nux-vomica seed tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9111 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V) POTASSIUM DICHROMATE 9 [hp_C] STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 9 [hp_C] FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 9 [hp_C] SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP 5 [hp_C] GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 9 [hp_C] Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) LACTOSE (UNII: J2B2A4N98G) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) Product Characteristics Color white Score no score Shape ROUND (Boiron) Size 9mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-9111-04 3 in 1 CARTON 03/20/2026 1 20 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/20/2026 Labeler - Boiron (282560473) Registrant - Boiron, Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-9111)


