Label: CHESTAL KIDS COLD AND COUGH HONEY- solanum dulcamara top, ferrosoferric phosphate, goldenseal, potassium dichromate, strychnos nux-vomica seed syrup
- NDC Code(s): 0220-9122-28
- 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 April 3, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
ACTIVE INGREDIENT
Active ingredients** (in each mL)
Dulcamara 5C HPUS (22.23 mg)
Ferrum phosphoricum 9C HPUS (22.23 mg)
Hydrastis canadensis 9C HPUS (22.23 mg)
(contains less than 10 -17 mg hydrastine and berberine alkaloids)
Kali bichromicum 9C HPUS (22.23 mg)
(contains less than 10 -17 mg chromium)
Nux vomica 9C HPUS (22.23 mg)
(contains less than 10 -18 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 (22.23 mg)……..............Relieves colds and cough worsened by exposure to damp cold
Ferrum phosphoricum 9C HPUS (22.23 mg)…Relieves colds with gradual onset, occasional minor sore throat, and dry, fitful cough
Hydrastis canadensis 9C HPUS (22.23 mg)….Relieves colds and cough associated with runny nose
Kali bichromicum 9C HPUS (22.23 mg).………Relieves nasal discharge
Nux vomica 9C HPUS (22.23 mg).………….....Relieves sneezing fits
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
-
STOP USE
Stop use and ask a doctor if
- sore throat worsens or persists for more than 2 days
- cough or nasal congestion worsens or lasts for more than 5 days in children under 12 years of age, comes back, or is accompanied by fever, rash, or a persistent headache
- new symptoms occur
These could be signs of a serious condition.
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- QUESTIONS
-
SPL UNCLASSIFIED SECTION
- do not use if glued carton end flaps are open or if the seal at base of cap is broken or missing
- retain carton for full drug facts
- contains 4 g of sugar per 5 mL
- dispose of 1 year after opening
- contains 0.000009% alcohol
Made in France
Distributed by Boiron Inc.
Newtown Square, PA 19073
MULTI-SYMPTOM
COLD & COUGH*
Nasal & Chest Congestion
Cough • Runny Nose*
- Day & Night Relief
- Kid-Friendly Taste
- Non-Drowsy
40 DOSES
99.999% ALCOHOL-FREE
6.7 fl oz
(200 mL)
COLD SYRUP
*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
-
INGREDIENTS AND APPEARANCE
CHESTAL KIDS COLD AND COUGH HONEY
solanum dulcamara top, ferrosoferric phosphate, goldenseal, potassium dichromate, strychnos nux-vomica seed syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0220-9122 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (SOLANUM DULCAMARA TOP - UNII:KPS1B1162N) SOLANUM DULCAMARA TOP 5 [hp_C] FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERROSOFERRIC PHOSPHATE 9 [hp_C] 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] GOLDENSEAL (UNII: ZW3Z11D0JV) (GOLDENSEAL - UNII:ZW3Z11D0JV) GOLDENSEAL 9 [hp_C] Inactive Ingredients Ingredient Name Strength HONEY (UNII: Y9H1V576FH) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) ALCOHOL (UNII: 3K9958V90M) CITRIC ACID (UNII: 2968PHW8QP) SUCROSE (UNII: C151H8M554) Product Characteristics Color Score Shape Size Flavor HONEY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0220-9122-28 1 in 1 CARTON 04/03/2026 1 1 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/03/2026 Labeler - Boiron (282560473) Registrant - Boiron, Inc. (014892269) Establishment Name Address ID/FEI Business Operations Boiron 282560473 manufacture(0220-9122)


