Chestal Cough and Cold
- Manufacturer
- Laboratoires Boiron | Boiron Inc. | Boiron
- Effective date
- 2024-02-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 8
- Source
- full-release
- Hydrated at
- 2026-06-01 02:26:04
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients** (in each mL)
Dulcamara 5C HPUS (0.13 mg)
Ferrum phosphoricum 9C HPUS (0.13 mg)
Hydrastis canadensis 9C HPUS (0.13 mg) (contains less than 10- 19 mg hydrastine and berberine alkaloids)
Kali bichromicum 9C HPUS (0.13mg) (contains less than 10 -19 mg chromium)
Nux vomica 9C HPUS (0.13mg) (contains less than 10 -20 mg strychnine alkaloids)
The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
OTC - PURPOSE SECTION
Purpose*
Dulcamara 5C HPUS (0.13mg) ... Relieves cold and coughs worsened by exposure to damp cold
Ferrum phosphoricum 9C HPUS (0.13mg) ... Relieves colds with gradual onset, minor sore throat, and dry, fitful cough
Hydrastis canadensis 9C HPUS (0.13mg) ... Relieves colds and coughs associated with runny nose
Kali bichromicum 9C HPUS (0.13mg) ... Relieves nasal discharge
Nux vomica 9C HPUS (0.13mg) ... Relieves sneezing fits
INDICATIONS & USAGE SECTION
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 SECTION
Do not use if you are allergic to any of this product's ingredients.
OTC - ASK DOCTOR SECTION
Ask a doctor before us 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).
OTC - STOP USE SECTION
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 or 7 days in adults, comes back, or is accompanied by fever, rash, or a persistent headache
- new symptoms occur.
These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
Age Adults and children 12 years of age and older Dose At the onset of symptoms, take 10 mL ± as needed, up to 8 times per day
Age Children 6 to under 12 years of age Dose At the onset of symptoms, take 5 mL ± as needed, up to 6 times per day
Age Children 4 to under 6 years of age Dose At the onset of symptoms, take 5 mL ± as needed, up to 3 times per day
Age Children under 4 years of age Dose Not recommended
±Use only with dosing cup provided.
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 this carton for full drug facts
contains 4.3 g of sugar per 5 mL
dispose of 1 year after opening
contains 0.000005% alcohol
Multi-symptom Cold & Cough Relief*
Cold & Cough Relief*
Nasal & Chest Congestion Cough, Runny Nose*
Non-Drowsy
Dye-Free
No Known Drug Interactions
6.7 fl. oz. (200 mL) cold syrup
20 Adult Doses
99.999% ALCOHOL FREE
*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.
INACTIVE INGREDIENT SECTION
alcohol, citric acid, purified water, sodium benzoate, sucrose
OTC - QUESTIONS SECTION
BoironUSA.com
Info@Boiron.com
1-800-BOIRON-1
(1-800-264-7661)
Distributed by Boiron, Inc.
Newtown Square, PA 19073
Made in France
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-9067-28 | Chestal Cough and Cold | 1 in 1 PACKAGE | SYRUP | 1 | 8 | |
| 0220-9067-28 | Chestal Cough and Cold | 200 mL in 1 BOTTLE | SYRUP | 200 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0220-9067 | CHESTAL COUGH AND COLD (SOLANUM DULCAMARA TOP, FERRUM PHOSPHORICUM, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED) SYRUP [LABORATOIRES BOIRON] | 8 | Current NDC, Legacy NDC, 2 package rows | 20240215_b347fb77-a46d-4c1e-ad40-c69e89387618.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| FERRUM PHOSPHORICUM | ACTIVE INGREDIENT | 91GQH8I5F7 | 4 | |
| GOLDENSEAL | ACTIVE INGREDIENT | ZW3Z11D0JV | 4 | |
| POTASSIUM DICHROMATE | ACTIVE INGREDIENT | T4423S18FM | 4 | |
| SOLANUM DULCAMARA TOP | ACTIVE INGREDIENT | KPS1B1162N | 4 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE INGREDIENT | 269XH13919 | 4 | |
| DICHROMATE ION | ACTIVE MOIETY | 9LKY4BFN2V | 4 | |
| FERROSOFERRIC PHOSPHATE | ACTIVE MOIETY | 91GQH8I5F7 | 4 | |
| GOLDENSEAL | ACTIVE MOIETY | ZW3Z11D0JV | 4 | |
| SOLANUM DULCAMARA TOP | ACTIVE MOIETY | KPS1B1162N | 4 | |
| STRYCHNOS NUX-VOMICA SEED | ACTIVE MOIETY | 269XH13919 | 4 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | 4 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | 4 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | 4 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 4 |
Products#
Every source-derived product name is available through these pages.
- Chestal Cough and Cold
- SOLANUM DULCAMARA TOP, FERRUM PHOSPHORICUM, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED
- CITRIC ACID MONOHYDRATE
- WATER
- SODIUM BENZOATE
- SUCROSE
- SOLANUM DULCAMARA TOP
- FERRUM PHOSPHORICUM
- FERROSOFERRIC PHOSPHATE
- GOLDENSEAL
- POTASSIUM DICHROMATE
- DICHROMATE ION
- STRYCHNOS NUX-VOMICA SEED
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-9067 | 0220-9067-28 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SUCROSE | C151H8M554 | IACT |
| SOLANUM DULCAMARA TOP | KPS1B1162N | ACTIB |
| FERRUM PHOSPHORICUM | 91GQH8I5F7 | ACTIB |
| GOLDENSEAL | ZW3Z11D0JV | ACTIB |
| POTASSIUM DICHROMATE | T4423S18FM | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| SUCROSE | SUCROSE | C151H8M554 | SYRUP / ORAL | 46400 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 mg | ||
| CITRIC ACID MONOHYDRATE | CITRIC ACID MONOHYDRATE | 2968PHW8QP | SYRUP / ORAL | 722 mg/5ml | ||
| SUCROSE | SUCROSE | C151H8M554 | SYRUP / ORAL | 46400 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 mg | ||
| CITRIC ACID MONOHYDRATE | CITRIC ACID MONOHYDRATE | 2968PHW8QP | SYRUP / ORAL | 722 mg/5ml |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Chestal Cough and Cold | SOLANUM DULCAMARA TOP, FERRUM PHOSPHORICUM, GOLDENSEAL, POTASSIUM DICHROMATE, STRYCHNOS NUX-VOMICA SEED | Laboratoires Boiron | b347fb77-a46d-4c1e-ad40-c69e89387618 | 2024-02-14 | Warnings | 0220-9067-28 0220-9067 00220906728 115c5a99-d67f-5009-e063-6294a90adf17 b347fb77-a46d-4c1e-ad40-c69e89387618 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.




