Chestal Child Honey
- Manufacturer
- Laboratoires Boiron | Boiron Inc. | Boiron
- Effective date
- 2026-10-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 12
- Source
- daily-update
- Hydrated at
- 2026-10-31 01:01:24
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients** (in each mL)
Antimonium tartaricum 6C HPUS (12.35 mg)
(contains less than 10 -11 mg antimony)
Bryonia 3C HPUS (12.35 mg)
Coccus cacti 3C HPUS (12.35 mg)
Drosera 3C HPUS (12.35 mg)
Ipecacuanha 3C HPUS (12.35 mg)
(contains less than 10 -6 mg emetine alkaloids)
Pulsatilla 6C HPUS (12.35 mg
Rumex crispus 6C HPUS (12.35 mg)
(contains less than 10 -13 mg anthraquinone glycosides)
Spongia tosta 3C HPUS (12.35 mg)
Sticta pulmonaria 3C HPUS (12.35 mg)
The designation "HPUS" means that the active ingredients in this product comply with monographs in the Homeopathic Pharmacopeia of the United States.
OTC - PURPOSE SECTION
Purpose*
Antimonium tartaricum 6C HPUS (12.35 mg)...........................................Helps loosen thick mucus
Bryonia 3C HPUS (12.35 mg).............................................................Relieves dry and painful cough
Coccus cacti 3C HPUS (12.35 mg)................Relieves cough associated with a tickling in the throat
Drosera 3C HPUS (12.35 mg).................................................Relieves barking cough worse at night
Ipecacuanha 3C HPUS (12.35 mg)........................................Relieves cough associated with nausea
Pulsatilla 6C HPUS (12.35 mg)................Relieves wet cough during the day becoming dry at night
Rumex crispus 6C HPUS (12.35 mg)....................................Relieves dry cough triggered by cold air
Spongia tosta 3C HPUS (12.35 mg)....................................Relieves dry, croupy, and barking cough
Sticta pulmonaria 3C HPUS (12.35 mg)........................................Relieves nighttime hacking cough
INDICATIONS & USAGE SECTION
Uses*
- temporarily relieves dry cough due to minor throat and bronchial irritation as may occur with a cold
- helps relieve chest congestion due to common colds by loosening mucus and thinning bronchial secretions to make coughs more productive
OTC - DO NOT USE SECTION
Do not use if your child is allergic to any of this product's ingredients.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if your child has
- persistent or chronic cough such as occurs with asthma
- cough that occurs with too much phlegm (mucus).
OTC - STOP USE SECTION
Stop use and ask a doctor if cough lasts for more than 7 days, comes back, or is accompanied by fever, rash, or a persistent headache. These could be a sign of a serious condition.
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
Children 4 to under 12 years of age At the onset of symptoms, take 5 mL ± up to 5 doses per day
Children under 4 years of age Not recommended
± Use only with dosing cup provided.
Do not use dosing cup with other products.
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 1 year after opening
contains 0.00007% alcohol
6.7 fl oz (200 ml) COUGH SYRUP
40 doses
Cough & Mucus*
Chest Congestion Dry, Fitful Cough*
Mutli-Symptom Cough & Mucus Relief*
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.
INACTIVE INGREDIENT SECTION
alcohol, citric acid, honey, purified water, sodium benzoate, sucrose
OTC - QUESTIONS SECTION
BoironUSA.com
info@boironusa.com
1-800-BOIRON-1 (
1-800-264-7661)
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ANTIMONY POTASSIUM TARTRATE | ACTIVE INGREDIENT | DL6OZ476V3 | 6 | |
| BRYONIA ALBA ROOT | ACTIVE INGREDIENT | T7J046YI2B | 6 | |
| DROSERA ROTUNDIFOLIA FLOWERING TOP | ACTIVE INGREDIENT | 75O014T1HG | 6 | |
| IPECAC | ACTIVE INGREDIENT | 62I3C8233L | 6 | |
| LOBARIA PULMONARIA | ACTIVE INGREDIENT | D1YM0P5Z2T | 6 | |
| PROTORTONIA CACTI | ACTIVE INGREDIENT | LZB7TFX1LT | 6 | |
| PULSATILLA VULGARIS | ACTIVE INGREDIENT | I76KB35JEV | 6 | |
| RUMEX CRISPUS ROOT | ACTIVE INGREDIENT | 9N1RM2S62C | 6 | |
| SPONGIA OFFICINALIS SKELETON, ROASTED | ACTIVE INGREDIENT | 1PIP394IID | 6 | |
| ANTIMONY CATION (3+) | ACTIVE MOIETY | 069647RPT5 | 6 | |
| BRYONIA ALBA ROOT | ACTIVE MOIETY | T7J046YI2B | 6 | |
| DROSERA ROTUNDIFOLIA FLOWERING TOP | ACTIVE MOIETY | 75O014T1HG | 6 | |
| IPECAC | ACTIVE MOIETY | 62I3C8233L | 6 | |
| LOBARIA PULMONARIA | ACTIVE MOIETY | D1YM0P5Z2T | 6 | |
| PROTORTONIA CACTI | ACTIVE MOIETY | LZB7TFX1LT | 6 | |
| PULSATILLA VULGARIS | ACTIVE MOIETY | I76KB35JEV | 6 | |
| RUMEX CRISPUS ROOT | ACTIVE MOIETY | 9N1RM2S62C | 6 | |
| SPONGIA OFFICINALIS SKELETON, ROASTED | ACTIVE MOIETY | 1PIP394IID | 6 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | 6 | |
| HONEY | INACTIVE INGREDIENT | Y9H1V576FH | 6 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | 6 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | 6 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 6 |
Products#
Every source-derived product name is available through these pages.
- Chestal for Children
- ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA
- BRYONIA ALBA ROOT
- PROTORTONIA CACTI
- DROSERA ROTUNDIFOLIA FLOWERING TOP
- IPECAC
- PULSATILLA VULGARIS
- RUMEX CRISPUS ROOT
- SPONGIA OFFICINALIS SKELETON, ROASTED
- LOBARIA PULMONARIA
- ANTIMONY POTASSIUM TARTRATE
- ANTIMONY CATION (3+)
- ALCOHOL
- HONEY
- SUCROSE
- WATER
- CITRIC ACID MONOHYDRATE
- SODIUM BENZOATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-9033 | 0220-9033-28, 0220-9033-16, 0220-9033-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
| PROTORTONIA CACTI | LZB7TFX1LT | ACTIB |
| DROSERA ROTUNDIFOLIA FLOWERING TOP | 75O014T1HG | ACTIB |
| IPECAC | 62I3C8233L | ACTIB |
| PULSATILLA VULGARIS | I76KB35JEV | ACTIB |
| RUMEX CRISPUS ROOT | 9N1RM2S62C | ACTIB |
| SPONGIA OFFICINALIS SKELETON, ROASTED | 1PIP394IID | ACTIB |
| LOBARIA PULMONARIA | D1YM0P5Z2T | ACTIB |
| ANTIMONY POTASSIUM TARTRATE | DL6OZ476V3 | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| HONEY | Y9H1V576FH | IACT |
| SUCROSE | C151H8M554 | IACT |
| WATER | 059QF0KO0R | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 11 | 2023-07-18 | full-release | 2026-06-01 02:21:53 |
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 |
|---|---|---|---|---|---|---|
| CITRIC ACID MONOHYDRATE | CITRIC ACID MONOHYDRATE | 2968PHW8QP | SYRUP / ORAL | 722 mg/5ml | ||
| CITRIC ACID MONOHYDRATE | CITRIC ACID MONOHYDRATE | 2968PHW8QP | SYRUP / ORAL | 722 mg/5ml | ||
| SUCROSE | SUCROSE | C151H8M554 | SYRUP / ORAL | 46400 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SYRUP / ORAL | 46400 mg | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 mg | ||
| 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 | ||
| SODIUM BENZOATE | SODIUM BENZOATE | OJ245FE5EU | SYRUP / ORAL | 80 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 |
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 |
|---|---|---|---|---|---|---|
| 00c80802-be3c-5fc8-e063-6394a90a7e86 | e4fb4963-31a4-44d7-bade-0eb695ac417f | 2023-07-18 | e4fb4963-31a4-44d7-bade-0eb695ac417f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.






