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#

ProductChestal for Children
Active ingredientBRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA FLOWERING TOP, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA, ANTIMONY POTASSIUM TARTRATE
Label structure12 sections

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

labellabellabellabelLABELLABELLABELLABELLABELLABELLABELLABELLABELLABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANTIMONY POTASSIUM TARTRATEACTIVE INGREDIENTDL6OZ476V36
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B6
DROSERA ROTUNDIFOLIA FLOWERING TOPACTIVE INGREDIENT75O014T1HG6
IPECACACTIVE INGREDIENT62I3C8233L6
LOBARIA PULMONARIAACTIVE INGREDIENTD1YM0P5Z2T6
PROTORTONIA CACTIACTIVE INGREDIENTLZB7TFX1LT6
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV6
RUMEX CRISPUS ROOTACTIVE INGREDIENT9N1RM2S62C6
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE INGREDIENT1PIP394IID6
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT56
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B6
DROSERA ROTUNDIFOLIA FLOWERING TOPACTIVE MOIETY75O014T1HG6
IPECACACTIVE MOIETY62I3C8233L6
LOBARIA PULMONARIAACTIVE MOIETYD1YM0P5Z2T6
PROTORTONIA CACTIACTIVE MOIETYLZB7TFX1LT6
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV6
RUMEX CRISPUS ROOTACTIVE MOIETY9N1RM2S62C6
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE MOIETY1PIP394IID6
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP6
HONEYINACTIVE INGREDIENTY9H1V576FH6
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EU6
SUCROSEINACTIVE INGREDIENTC151H8M5546
WATERINACTIVE INGREDIENT059QF0KO0R6

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-90330220-9033-28, 0220-9033-16, 0220-9033-15

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
112023-07-18full-release2026-06-01 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.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSYRUP / ORAL722 mg/5mlExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSYRUP / ORAL722 mg/5mlExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUSYRUP / ORAL80 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUSYRUP / ORAL80 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSYRUP / ORAL722 mg/5mlExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUSYRUP / ORAL80 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUSYRUP / ORAL80 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
CITRIC ACID MONOHYDRATECITRIC ACID MONOHYDRATE2968PHW8QPSYRUP / ORAL722 mg/5mlExact identifier — unii+route+dosage form
4 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
00c80802-be3c-5fc8-e063-6394a90a7e86e4fb4963-31a4-44d7-bade-0eb695ac417f2023-07-18Exact identifier
spl set id: e4fb4963-31a4-44d7-bade-0eb695ac417f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.