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
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
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.
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.
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
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
Ask a doctor before use in children under 2 years of age.
symptoms persist for more than 7 days or worsen.
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.
do not use if the label sealing the clear tube cap is broken or missing
lactose, sucrose
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
*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.
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0220-9061-42 | 2023-01-30 | C162847 | 48780-1 | 9d75b9d1-12cf-f424-e053-dadaa90a57ce | Childrens Sabadil |
| 0220-9061-42 | 2020-02-26 | C162847 | 48780-1 | 9d75b9d1-12cf-f424-e053-dadaa90a57ce | Childrens Sabadil |
| 0220-9061-42 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-12cf-f424-e053-dadaa90a57ce | Childrens Sabadil |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-9061-41 | Childrens Sabadil | 80 in 1 TUBE | PELLET | 80 | 8 | |
| 0220-9061-42 | Childrens Sabadil | 2 in 1 PACKAGE | PELLET | 2 | 8 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0220-9061 | CHILDRENS SABADIL (ONION, AMBROSIA ARTEMISIIFOLIA, HISTAMINE DIHYDROCHLORIDE, SCHOENOCAULON OFFICINALE SEED, EUPHRASIA STRICTA, SOLIDAGO VIRGAUREA FLOWERING TOP) PELLET [LABORATOIRES BOIRON] | 8 | Legacy NDC, 2 package rows | 20201104_edc1bcd5-fcad-40fa-94b0-12518434b105.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| AMBROSIA ARTEMISIIFOLIA | ACTIVE INGREDIENT | 9W34L2CQ9A | 4 | |
| EUPHRASIA STRICTA | ACTIVE INGREDIENT | C9642I91WL | 4 | |
| HISTAMINE DIHYDROCHLORIDE | ACTIVE INGREDIENT | 3POA0Q644U | 4 | |
| ONION | ACTIVE INGREDIENT | 492225Q21H | 4 | |
| SCHOENOCAULON OFFICINALE SEED | ACTIVE INGREDIENT | 6NAF1689IO | 4 | |
| SOLIDAGO VIRGAUREA FLOWERING TOP | ACTIVE INGREDIENT | 5405K23S50 | 4 | |
| AMBROSIA ARTEMISIIFOLIA | ACTIVE MOIETY | 9W34L2CQ9A | 4 | |
| EUPHRASIA STRICTA | ACTIVE MOIETY | C9642I91WL | 4 | |
| HISTAMINE | ACTIVE MOIETY | 820484N8I3 | 4 | |
| ONION | ACTIVE MOIETY | 492225Q21H | 4 | |
| SCHOENOCAULON OFFICINALE SEED | ACTIVE MOIETY | 6NAF1689IO | 4 | |
| SOLIDAGO VIRGAUREA FLOWERING TOP | ACTIVE MOIETY | 5405K23S50 | 4 | |
| LACTOSE | INACTIVE INGREDIENT | J2B2A4N98G | 4 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | 4 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0220-9061 | 0220-9061-41, 0220-9061-42 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| LACTOSE | J2B2A4N98G | IACT |
| ONION | 492225Q21H | ACTIB |
| AMBROSIA ARTEMISIIFOLIA | 9W34L2CQ9A | ACTIB |
| HISTAMINE DIHYDROCHLORIDE | 3POA0Q644U | ACTIB |
| SCHOENOCAULON OFFICINALE SEED | 6NAF1689IO | ACTIB |
| EUPHRASIA STRICTA | C9642I91WL | ACTIB |
| SOLIDAGO VIRGAUREA FLOWERING TOP | 5405K23S50 | ACTIB |
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 | POWDER, FOR SOLUTION / ORAL | 38666 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SUSPENSION / ORAL | 48209 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | GRANULE, FOR SUSPENSION / ORAL | 512.5 mg/5ml | ||
| SUCROSE | SUCROSE | C151H8M554 | SOLUTION / ORAL | 70000 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, DELAYED RELEASE / ORAL | 295.33 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, CHEWABLE / ORAL | 1412 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, EMULSION / INTRAVENOUS | 970 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, DELAYED RELEASE / ORAL | 160 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, FILM COATED / ORAL | 145 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE, EXTENDED RELEASE / ORAL | 619 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | SUSPENSION/ DROPS / ORAL | 3750 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION / INTRAVENOUS | 203.5 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, COATED / ORAL | 332.05 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE / RESPIRATORY (INHALATION) | 44.4 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / BUCCAL | 296.7 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | LOZENGE / TRANSMUCOSAL | 1255 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, SUSPENSION, EXTENDED RELEASE / SUBCUTANEOUS | 1 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, FILM COATED / ORAL | 590 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, EXTENDED RELEASE / ORAL | 400 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | POWDER / ORAL | 27768 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | PASTILLE / ORAL | 426 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET / SUBLINGUAL | 109 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | SOLUTION / ORAL | 1682 mg/15ml | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET / RECTAL | 20 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET / ORAL | 4249 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, POWDER, FOR SOLUTION / INTRAVENOUS | 133 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | LIQUID / ORAL | 37500 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 620 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRACAVITARY | 193.8 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, SOLUTION / INTRAVENOUS | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | SYRUP / ORAL | 46400 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, SOLUTION / INTRAVENOUS | 0.45 %w/v | ||
| SUCROSE | SUCROSE | C151H8M554 | SUPPOSITORY / RECTAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE, COATED PELLETS / ORAL | 135.2 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, EFFERVESCENT / ORAL | 96.5 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, POWDER, FOR SOLUTION / SUBCUTANEOUS | 133 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, EXTENDED RELEASE / ORAL | 284.54 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET / BUCCAL | 109 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, SUSPENSION, LIPOSOMAL / INTRAVENOUS | 9.4 %w/v | ||
| SUCROSE | SUCROSE | C151H8M554 | CAPSULE, COATED PELLETS / ORAL | 59.8 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | POWDER / RESPIRATORY (INHALATION) | 90 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, POWDER, FOR SUSPENSION / INTRAVENOUS | 900 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | ELIXIR / ORAL | 18000 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORAL | 18790 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / SUBCUTANEOUS | 308 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | TABLET, SUGAR COATED / ORAL | NA | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CONCENTRATE / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | TABLET, FILM COATED, EXTENDED RELEASE / ORAL | 119.12 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | INJECTION, POWDER, FOR SOLUTION / INTRAMUSCULAR | 133 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | TROCHE / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | DROPS / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | CONCENTRATE / ORAL | 4800 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE, EXTENDED RELEASE / ORAL | 120 mg | ||
| SUCROSE | SUCROSE | C151H8M554 | GRANULE / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | POWDER, FOR SUSPENSION / ORAL | 40017 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | FILM, EXTENDED RELEASE / TRANSDERMAL | 675 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | SOLUTION / RECTAL | 8 %w/v | ||
| SUCROSE | SUCROSE | C151H8M554 | INJECTION / SUBCUTANEOUS | 47.75 mg | ||
| LACTOSE | LACTOSE | J2B2A4N98G | CAPSULE, COATED, EXTENDED RELEASE / ORAL | NA | ||
| SUCROSE | SUCROSE | C151H8M554 | LOZENGE / BUCCAL | NA |
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 |
|---|---|---|---|---|---|---|
| b32410f8-af85-789d-e053-2a95a90a3def | edc1bcd5-fcad-40fa-94b0-12518434b105 | 2020-11-02 | Warnings | b32410f8-af85-789d-e053-2a95a90a3def edc1bcd5-fcad-40fa-94b0-12518434b105 |
Adverse event summaries are temporarily unavailable. Other product information remains available.