MEDULLA OSSIS SUIS

Manufacturer: BOIRON | BOIRON, INC.
Effective date: 2023-11-14
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 02:24:05

Label at a glance#

ProductMEDULLA OSSIS SUIS

Active ingredientSUS SCROFA BONE MARROW

Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

MEDULLA OSSIS SUIS HPUS

OTC - PURPOSE SECTION

Arthritic pain in spine

INDICATIONS & USAGE SECTION

Arthritic pain in spine

OTC - STOP USE SECTION

STOP USE IF SYMPTOMS PERSIST FOR MORE THAN 3 DAYS OR WORSEN

OTC - PREGNANCY OR BREAST FEEDING SECTION

ASK A HEALTH PROFESSIONAL BEFORE USE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION SECTION

5 PELLETS 3 TIMES A DAY UNTIL SYMPTOMS ARE RELIEVED

SPL UNCLASSIFIED SECTION

DO NOT USE IF PELLET DISPENSER IS BROKEN.

CONTAINS APPROX. 80 PELLETS

INACTIVE INGREDIENT SECTION

LACTOSE, SUCROSE

OTC - QUESTIONS SECTION

1-800-BOIRON-1

Newtown Square, PA 19073-3267

info@boironusa.com

SPL UNCLASSIFIED SECTION

These "Uses" have not been evaluated by the FDA.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0220-3329-41	2023-11-14	C162847	48780-1	f386c649-b76f-0266-e053-dadaa90a7c1a	MEDULLA OSSIS SUIS
0220-3329-41	2023-01-30	C162847	48780-1	f386c649-b76f-0266-e053-dadaa90a7c1a	MEDULLA OSSIS SUIS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0220-3329-41	MEDULLA OSSIS SUIS	8 [hp_X] in 1 TUBE	PELLET	8		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0220-3329	MEDULLA OSSIS SUIS (SUS SCROFA BONE MARROW) PELLET [BOIRON]	3	Current NDC, Legacy NDC, 1 package rows	20231115_61e659a2-f4af-42db-e053-2991aa0ab8f5.zip

Products#

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

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

MEDULLA OSSIS SUIS
SUS SCROFA BONE MARROW
SUCROSE
LACTOSE, UNSPECIFIED FORM
ANHYDROUS LACTOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0220-3329	0220-3329-41

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
SUS SCROFA BONE MARROW	VP2CN2G7Y8	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MEDULLA OSSIS SUIS	SUS SCROFA BONE MARROW	BOIRON	61e659a2-f4af-42db-e053-2991aa0ab8f5	2023-11-14		Exact identifier ndc (package): 0220-3329-41 ndc (product): 0220-3329 ndc11 (package): 00220332941 spl id: 0a1f531e-55e6-7573-e063-6294a90aaa48 spl set id: 61e659a2-f4af-42db-e053-2991aa0ab8f5

Reported adverse events (FAERS/openFDA)#

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