Bryonia

Manufacturer
Boiron | Boiron, Inc.
Effective date
2026-01-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:36:39

Label at a glance#

ProductBryonia
Active ingredientBRYONIA ALBA ROOT
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient** (in each pellet)

Bryonia 30C HPUS (0.44 mg)

The letters "HPUS" indicate that the component in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

OTC - PURPOSE SECTION

Purpose*

Relieves muscle and joint pain improved by rest

INDICATIONS & USAGE SECTION

temporarily relieves symptoms of muscle and joint pain including:

  • stiffness
  • pain improved by rest
  • minor arthritis pain

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen, new symptoms occur, or if redness or swelling is present, as these could be signs of 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 overdose, get medical help or contact a Poison Control Center right away.

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

BoironUSA.com Info@boiron.com

1-800-BOIRON-1 (1-800-264-7661)
Distributed by Boiron, Inc.

Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

Do not use if pellet dispenser seal is broken.
Do not use if glued carton end flaps are open or if pellet dispenser seal is broken.

1 Tube approx 80 pellets

3 Tubes approx 80 pellets 16 Doses per tube Total 240 pellets

How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed. Remove cap and pour pellets under the tongue.

Pain Relief*

Joint Pain Muscle Aches Arthritis Pain*

No known drug interactions

Joint & Muscle Pain Relief*

*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

LABELLABELLABELLABELLABELLABELLABELLABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0944-412023-04-11C16284748780-1f386c649-aa58-0266-e053-dadaa90a7c1aBryonia 30C
0220-0944-432023-04-11C16284748780-1f386c649-aa58-0266-e053-dadaa90a7c1aBryonia 30C
0220-0944-412023-01-30C16284748780-1f386c649-aa58-0266-e053-dadaa90a7c1aBryonia 30C
0220-0944-432023-01-30C16284748780-1f386c649-aa58-0266-e053-dadaa90a7c1aBryonia 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0944-41Bryonia30 [hp_C] in 1 TUBEPELLET304
0220-0944-43Bryonia3 in 1 BOXPELLET34
0220-0944-43Bryonia30 [hp_C] in 1 TUBEPELLET304

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-09440220-0944-41, 0220-0944-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

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
BryoniaBRYONIA ALBA ROOTBoiron848a1836-b86a-fc68-e053-2991aa0af6a52026-01-02Exact identifier
ndc (package): 0220-0944-43
ndc (package): 0220-0944-41
ndc (product): 0220-0944
ndc11 (package): 00220094443
ndc11 (package): 00220094441
spl id: 476d0a29-86a1-aa50-e063-6294a90a35bf
spl set id: 848a1836-b86a-fc68-e053-2991aa0af6a5

Reported adverse events (FAERS/openFDA)#

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