Chestal

Manufacturer
Laboratoires Boiron | Boiron Inc. | Boiron
Effective date
2023-09-11
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-06-01 02:22:14

Label at a glance#

ProductChestal
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 structure13 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 letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Antimonium tartaricum 6C HPUS ... Helps loosen thick mucus

Bryonia 3C HPUS ... Relieves dry and painful cough

Coccus cacti 3C HPUS ... Relieves cough associated with a tickling in the throat

Drosera 3C HPUS ... Relieves barking cough worse at night

Ipecacuanha 3C HPUS ... Relieves cough associated with nausea

Pulsatilla 6C HPUS ... Relieves wet cough during the day becoming dry at night

Rumex crispus 6C HPUS ... Relieves dry cough triggered by cold air

Spongia tosta 3C HPUS ... Relieves dry, croupy and barking cough

Sticta pulmonaria 3C HPUS ... Relieves nighttime hacking cough

INDICATIONS & USAGE SECTION

Uses*

temporarily relieves dry cough due to minor throat and bronchial irritation as may occur with 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 you are allergic to any of this product's ingredients.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

cough that lasts or is chronic 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 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 - 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 accidental overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older - At the onset of symptoms, take 10 mL + every 2 hours, up to 8 doses per day

Children 4 to 11 years of age - At the onset of symptoms, take 5 mL+ every 2 hours, 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.

INACTIVE INGREDIENT SECTION

alcohol, citric acid, honey, purified water, sodium benzoate, sucrose

OTC - QUESTIONS SECTION

Questions, Comments

Boironusa.com
info@boironusa.com

1-800-BOIRON-1 (1-800-264-7661)

Distributed by Boiron, Inc.
Newtown Square, PA 19073-3267

Made in France

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 directions

contains 4 g of sugar per 5 mL

contains 0.00007% alcohol

dispose of 1 year after opening

6.7 fl oz (200 mL) cough syrup

20 Adult Doses

Multi-Symptom Cough & Mucus Relief*

Cough & Mucus Relief*

Chest Congestion, Dry, Fitful Cough*

Made with Real Acacia Honey

Day & Night Relief

Non-Drowsy

*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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabellabellabellabellabellabellabelboxbox

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9032-15Chestal125 mL in 1 BOTTLESYRUP12514
0220-9032-16Chestal250 mL in 1 BOTTLESYRUP25014
0220-9032-28Chestal200 mL in 1 BOTTLESYRUP20014

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9032CHESTAL (ANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIA) SYRUP [LABORATOIRES BOIRON]14Current NDC, Legacy NDC, 3 package rows20230912_76589f60-0f09-4d7a-8aaa-f1965df1fe9d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ANTIMONY POTASSIUM TARTRATEACTIVE INGREDIENTDL6OZ476V38
BRYONIA ALBA ROOTACTIVE INGREDIENTT7J046YI2B8
DROSERA ROTUNDIFOLIA FLOWERING TOPACTIVE INGREDIENT75O014T1HG8
IPECACACTIVE INGREDIENT62I3C8233L8
LOBARIA PULMONARIAACTIVE INGREDIENTD1YM0P5Z2T8
PROTORTONIA CACTIACTIVE INGREDIENTLZB7TFX1LT8
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV8
RUMEX CRISPUS ROOTACTIVE INGREDIENT9N1RM2S62C8
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE INGREDIENT1PIP394IID8
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT58
BRYONIA ALBA ROOTACTIVE MOIETYT7J046YI2B8
DROSERA ROTUNDIFOLIA FLOWERING TOPACTIVE MOIETY75O014T1HG8
IPECACACTIVE MOIETY62I3C8233L8
LOBARIA PULMONARIAACTIVE MOIETYD1YM0P5Z2T8
PROTORTONIA CACTIACTIVE MOIETYLZB7TFX1LT8
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV8
RUMEX CRISPUS ROOTACTIVE MOIETY9N1RM2S62C8
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE MOIETY1PIP394IID8
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QP8
HONEYINACTIVE INGREDIENTY9H1V576FH8
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EU8
SUCROSEINACTIVE INGREDIENTC151H8M5548
WATERINACTIVE INGREDIENT059QF0KO0R8

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
0220-90320220-9032-28, 0220-9032-16, 0220-9032-15

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 · Source PDF

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
SUCROSESUCROSEC151H8M554SYRUP / ORAL46400 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
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
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
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
SODIUM BENZOATESODIUM BENZOATEOJ245FE5EUSYRUP / ORAL80 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
ChestalANTIMONY POTASSIUM TARTRATE, BRYONIA ALBA ROOT, PROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, IPECAC, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, PONGIA OFFICINALIS SKELETON, ROASTED, LOBARIA PULMONARIALaboratoires Boiron76589f60-0f09-4d7a-8aaa-f1965df1fe9d2023-09-11Exact identifier
ndc (package): 0220-9032-16
ndc (package): 0220-9032-28
ndc (package): 0220-9032-15
ndc (product): 0220-9032
ndc11 (package): 00220903216
ndc11 (package): 00220903228
ndc11 (package): 00220903215
spl id: 05173f5f-6763-be69-e063-6394a90a8852
spl set id: 76589f60-0f09-4d7a-8aaa-f1965df1fe9d

Reported adverse events (FAERS/openFDA)#

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