Bryonia
- Manufacturer
- Boiron | Boiron, Inc.
- Effective date
- 2026-01-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:36:40
Label at a glance#
ProductBryonia
Active ingredientBRYONIA ALBA ROOT
Label structure10 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Bryonia 30X HPUS
Active ingredient**: See product name on front panel (contains 0.443 mg of the active ingredient per pellet).
INDICATIONS & USAGE SECTION
Relieves muscle and joint pain improved by rest *
Uses: See symptoms on front panel.
OTC - STOP USE SECTION
Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.
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.
DOSAGE & ADMINISTRATION SECTION
Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
INACTIVE INGREDIENT SECTION
lactose, sucrose
OTC - QUESTIONS SECTION
1-800-BOIRON-1 (1-800-264-7661),
BoironUSA.com Info@boiron.com
Distributed by Boiron, Inc. Newtown Square, PA 19073
SPL UNCLASSIFIED SECTION
Do not use if pellet dispenser seal is broken.
Contains approx 80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*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
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 0220-0949-41 | 2023-11-09 | C162847 | 48780-1 | f386c649-d93f-0266-e053-dadaa90a7c1a | Bryonia 30X |
| 0220-0949-41 | 2023-01-30 | C162847 | 48780-1 | f386c649-d93f-0266-e053-dadaa90a7c1a | Bryonia 30X |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-0949-41 | Bryonia | 30 [hp_X] in 1 TUBE | PELLET | 30 | 3 |
Products#
Every source-derived product name is available through these pages.
- Bryonia
- BRYONIA ALBA ROOT
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-0949 | 0220-0949-41 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| SUCROSE | C151H8M554 | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| Bryonia | BRYONIA ALBA ROOT | Boiron | 8502ac84-1022-e92d-e053-2991aa0a38bc | 2026-01-05 | 0220-0949-41 0220-0949 00220094941 47aa1836-3946-0917-e063-6294a90a652f 8502ac84-1022-e92d-e053-2991aa0a38bc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.