Childrens Sabadil

Manufacturer
Laboratoires Boiron | Boiron Inc. | Boiron
Effective date
2020-11-02
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 02:13:27

Label at a glance#

ProductChildrens Sabadil
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA, HISTAMINE DIHYDROCHLORIDE, SCHOENOCAULON OFFICINALE SEED, EUPHRASIA STRICTA, SOLIDAGO VIRGAUREA FLOWERING TOP
Label structure10 sections

Indications and uses

temporarily relieves on or more of these symptoms of hay fever or other uppper respiratory allergies: itchy and watery eyes sneezing runny nose itchy throat and nose

Dosage and administration

Children 2 years of age and older: At the onser of symptoms, dissolve 5 pellets under the tounge every 15 minutes for 1 hour. Then, dissolve 5 pellets under the tounge 3 times a day until symptoms are releived. Children under 2 years of age: Ask a doctor.

Label contents#

Full prescribing information#

Active Ingredients**

OTC - ACTIVE INGREDIENT SECTION

Allium cepa 5C HPUS
Ambrosia artemisiaefolia 5C HPUS
Euphrasia officinalis 5C HPUS
Histaminum hydrochloricum 9C HPUS
Sabadilla 5C HPUS
Solidago virgaurea 5C HPUS

The letters HPUS indicate that this ingredient is officially included in the Homeopathic Pharmacopoeia of the United States.

Purpose*

OTC - PURPOSE SECTION

Allium cepa 5C HPUS ..... Relieves runny nouse associated with allergies
Ambrosia artemisiaefolia 5C HPUS ..... Relieves spasmodic cough associated with hay fever
Histaminum hydrochloricum 9C HPUS ..... Relieves symptoms of allergic conditions
Euphrasia officinalis 5C HPUS ..... Relieves burning, irritated eyes
Sabadilla 5C HPUS ..... Relieves sneezing associated with allergies
Solidago virgaurea 5C HPUS ..... Relieves abundant nasal discharge

Uses*

INDICATIONS & USAGE SECTION

temporarily relieves on or more of these symptoms of hay fever or other uppper respiratory allergies:
itchy and watery eyes
sneezing
runny nose
itchy throat and nose

Warnings

WARNINGS SECTION

OTC - ASK DOCTOR SECTION

Ask a doctor before use in children under 2 years of age.

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms persist for more than 7 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Children 2 years of age and older: At the onser of symptoms, dissolve 5 pellets under the tounge every 15 minutes for 1 hour. Then, dissolve 5 pellets under the tounge 3 times a day until symptoms are releived.
Children under 2 years of age: Ask a doctor.

Other information

SPL UNCLASSIFIED SECTION

do not use if the label sealing the clear tube cap is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

lactose, sucrose

Questions, Comments?

OTC - QUESTIONS SECTION

BoironUSA.com
info@boiron.com
1-800-BOIRON-1 (1-800-264-7661)
Distributed by Boiron Inc., 6 Campus Boulevard, Newtown Square, PA 19073-3267

Notes:

SPL UNCLASSIFIED SECTION

*These "Uses" have not been evaluated by the Food And Drug Administration.
**C, K, CK and X are homeopathic dilutions: see BoironUSA.com/info for details.

Principle Display Panel - Childrens Sabadil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principle Display Panel - Childrens SabadilPrinciple Display Panel - Childrens Sabadil

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-9061-422023-01-30C16284748780-19d75b9d1-12cf-f424-e053-dadaa90a57ceChildrens Sabadil
0220-9061-422020-02-26C16284748780-19d75b9d1-12cf-f424-e053-dadaa90a57ceChildrens Sabadil
0220-9061-422020-01-31C16284748780-19d75b9d1-12cf-f424-e053-dadaa90a57ceChildrens Sabadil

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-9061-41Childrens Sabadil80 in 1 TUBEPELLET808
0220-9061-42Childrens Sabadil2 in 1 PACKAGEPELLET28

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-9061CHILDRENS SABADIL (ONION, AMBROSIA ARTEMISIIFOLIA, HISTAMINE DIHYDROCHLORIDE, SCHOENOCAULON OFFICINALE SEED, EUPHRASIA STRICTA, SOLIDAGO VIRGAUREA FLOWERING TOP) PELLET [LABORATOIRES BOIRON]8Legacy NDC, 2 package rows20201104_edc1bcd5-fcad-40fa-94b0-12518434b105.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMBROSIA ARTEMISIIFOLIAACTIVE INGREDIENT9W34L2CQ9A4
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WL4
HISTAMINE DIHYDROCHLORIDEACTIVE INGREDIENT3POA0Q644U4
ONIONACTIVE INGREDIENT492225Q21H4
SCHOENOCAULON OFFICINALE SEEDACTIVE INGREDIENT6NAF1689IO4
SOLIDAGO VIRGAUREA FLOWERING TOPACTIVE INGREDIENT5405K23S504
AMBROSIA ARTEMISIIFOLIAACTIVE MOIETY9W34L2CQ9A4
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WL4
HISTAMINEACTIVE MOIETY820484N8I34
ONIONACTIVE MOIETY492225Q21H4
SCHOENOCAULON OFFICINALE SEEDACTIVE MOIETY6NAF1689IO4
SOLIDAGO VIRGAUREA FLOWERING TOPACTIVE MOIETY5405K23S504
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G4
SUCROSEINACTIVE INGREDIENTC151H8M5544

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-90610220-9061-41, 0220-9061-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

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 2 · 84 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SUCROSESUCROSEC151H8M554POWDER, FOR SOLUTION / ORAL38666 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SUSPENSION / ORAL48209 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GGRANULE, FOR SUSPENSION / ORAL512.5 mg/5mlExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SOLUTION / ORAL70000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET, DELAYED RELEASE / ORAL295.33 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, CHEWABLE / ORAL1412 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, EMULSION / INTRAVENOUS970 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, DELAYED RELEASE / ORAL160 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET, FILM COATED / ORAL145 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554CAPSULE, EXTENDED RELEASE / ORAL619 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SUSPENSION/ DROPS / ORAL3750 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GINJECTION / INTRAVENOUS203.5 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, COATED / ORAL332.05 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GCAPSULE / RESPIRATORY (INHALATION)44.4 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / BUCCAL296.7 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554LOZENGE / TRANSMUCOSAL1255 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS1 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, FILM COATED / ORAL590 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, EXTENDED RELEASE / ORAL400 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554POWDER / ORAL27768 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554PASTILLE / ORAL426 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET / SUBLINGUAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GSOLUTION / ORAL1682 mg/15mlExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / RECTAL20 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET / ORAL4249 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GINJECTION, POWDER, FOR SOLUTION / INTRAVENOUS133 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554LIQUID / ORAL37500 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, FILM COATED, EXTENDED RELEASE / ORAL620 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARY193.8 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, SOLUTION / INTRAVENOUSNAExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SYRUP / ORAL46400 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GINJECTION, SOLUTION / INTRAVENOUS0.45 %w/vExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554SUPPOSITORY / RECTALNAExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GCAPSULE, COATED PELLETS / ORAL135.2 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, EFFERVESCENT / ORAL96.5 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GINJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS133 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET, EXTENDED RELEASE / ORAL284.54 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET / BUCCAL109 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS9.4 %w/vExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554CAPSULE, COATED PELLETS / ORAL59.8 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GPOWDER / RESPIRATORY (INHALATION)90 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS900 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554ELIXIR / ORAL18000 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL18790 mgExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS308 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET, SUGAR COATED / ORALNAExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GCONCENTRATE / ORALNAExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET, FILM COATED, EXTENDED RELEASE / ORAL119.12 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GINJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR133 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TROCHE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554DROPS / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554CONCENTRATE / ORAL4800 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GCAPSULE, EXTENDED RELEASE / ORAL120 mgExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554GRANULE / ORALNAExact identifier — unii candidate
48 equally ranked IID candidates
SUCROSESUCROSEC151H8M554POWDER, FOR SUSPENSION / ORAL40017 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GFILM, EXTENDED RELEASE / TRANSDERMAL675 mgExact identifier — unii candidate
36 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GSOLUTION / RECTAL8 %w/vExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554INJECTION / SUBCUTANEOUS47.75 mgExact identifier — unii candidate
48 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GCAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
36 equally ranked IID candidates
SUCROSESUCROSEC151H8M554LOZENGE / BUCCALNAExact identifier — unii candidate
48 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
b32410f8-af85-789d-e053-2a95a90a3defedc1bcd5-fcad-40fa-94b0-12518434b1052020-11-02WarningsExact identifier
spl id: b32410f8-af85-789d-e053-2a95a90a3def
spl set id: edc1bcd5-fcad-40fa-94b0-12518434b105

Reported adverse events (FAERS/openFDA)#

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