Indications and uses
For temporary relief of minor tearing, drawing pains in the muscles and fibrous tissues, pain in the lower part of the back with burning, pain between shoulder blades; and rheumatism in lumbar region.
Osteoforce
- Manufacturer
- BioActive Nutritional, Inc. | Apotheca Company
- Effective date
- 2025-04-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 02:32:59
Label at a glance#
ProductOsteoforce
Active ingredientSUS SCROFA BONE MARROW, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CALCIUM FLUORIDE, CAUSTICUM, ANAMIRTA COCCULUS SEED, RHODODENDRON TOMENTOSUM LEAFY TWIG, PHOSPHORIC ACID, TOXICODENDRON PUBESCENS LEAF
Label structure9 sections
Dosage and administration
• 10 drops orally, 3 times a day. • Consult a health care professional for use in children under 12 years of age.
Contacts and useful links#
Label contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Calcarea Carbonica 12X, Calcarea Fluorica 12X, Causticum 12X, Cocculus Indicus 12X, Ledum Palustre 12X, Medulla Ossis Suis 6X, Phosphoricum Acidum 12X, Rhus Tox 12X.
PURPOSE:
Calcarea Carbonica - cramps,** Calcarea Fluorica – joint pain,** Causticum - inflammation,** Cocculus Indicus - dizziness,** Ledum Palustre - swelling,** Medulla Ossis Suis – arthritic pain,** Phosphoricum Acidum - weakness,** Rhus Tox – joint pain**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
USES:
For temporary relief of minor tearing, drawing pains in the muscles and fibrous tissues, pain in the lower part of the back with burning, pain between shoulder blades; and rheumatism in lumbar region.
WARNINGS:
If pregnant or breast-feeding, ask a health care professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing.
Store in a cool, dry place.
KEEP OUT OF REACH OF CHILDREN:
In case of overdose, get medical help or contact a Poison Control Center right away.
DIRECTIONS:
• 10 drops orally, 3 times a day.
• Consult a health care professional for use in children under 12 years of age.
INACTIVE INGREDIENTS:
Demineralized Water, 25% Ethanol
QUESTIONS:
Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com
1-800-288-9525
PACKAGE LABEL DISPLAY:
BIOActive Nutritional
OSTEOFORCE
HOMEOPATHIC
1 FL OZ (30 ml)
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43857-0351-1 | Osteoforce | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43857-0351 | OSTEOFORCE (MEDULLA OSSIS SUIS, CALCAREA CARBONICA, CALCAREA FLUORICA, CAUSTICUM, COCCULUS INDICUS, LEDUM PALUSTRE, PHOSPHORICUM ACIDUM, RHUS TOX) LIQUID [BIOACTIVE NUTRITIONAL, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250403_15dfc9a0-b974-414f-bf06-4c508f9c413d.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ANAMIRTA COCCULUS SEED | ACTIVE INGREDIENT | 810258W28U | 1 | |
| CALCIUM FLUORIDE | ACTIVE INGREDIENT | O3B55K4YKI | 1 | |
| CAUSTICUM | ACTIVE INGREDIENT | DD5FO1WKFU | 1 | |
| LEDUM PALUSTRE TWIG | ACTIVE INGREDIENT | 877L01IZ0P | 1 | |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | ACTIVE INGREDIENT | 2E32821G6I | 1 | |
| PHOSPHORIC ACID | ACTIVE INGREDIENT | E4GA8884NN | 1 | |
| SUS SCROFA BONE MARROW | ACTIVE INGREDIENT | VP2CN2G7Y8 | 1 | |
| TOXICODENDRON PUBESCENS LEAF | ACTIVE INGREDIENT | 6IO182RP7A | 1 | |
| ANAMIRTA COCCULUS SEED | ACTIVE MOIETY | 810258W28U | 1 | |
| CAUSTICUM | ACTIVE MOIETY | DD5FO1WKFU | 1 | |
| FLUORIDE ION | ACTIVE MOIETY | Q80VPU408O | 1 | |
| LEDUM PALUSTRE TWIG | ACTIVE MOIETY | 877L01IZ0P | 1 | |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | ACTIVE MOIETY | 2E32821G6I | 1 | |
| PHOSPHORIC ACID | ACTIVE MOIETY | E4GA8884NN | 1 | |
| SUS SCROFA BONE MARROW | ACTIVE MOIETY | VP2CN2G7Y8 | 1 | |
| TOXICODENDRON PUBESCENS LEAF | ACTIVE MOIETY | 6IO182RP7A | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Osteoforce
- Medulla Ossis Suis, Calcarea Carbonica, Calcarea Fluorica, Causticum, Cocculus Indicus, Ledum Palustre, Phosphoricum Acidum, Rhus Tox
- SUS SCROFA BONE MARROW
- OYSTER SHELL CALCIUM CARBONATE, CRUDE
- CALCIUM FLUORIDE
- FLUORIDE ION
- CAUSTICUM
- ANAMIRTA COCCULUS SEED
- RHODODENDRON TOMENTOSUM LEAFY TWIG
- PHOSPHORIC ACID
- TOXICODENDRON PUBESCENS LEAF
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43857-0351 | 43857-0351-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUS SCROFA BONE MARROW | VP2CN2G7Y8 | ACTIB |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 2E32821G6I | ACTIB |
| CALCIUM FLUORIDE | O3B55K4YKI | ACTIB |
| CAUSTICUM | DD5FO1WKFU | ACTIB |
| ANAMIRTA COCCULUS SEED | 810258W28U | ACTIB |
| RHODODENDRON TOMENTOSUM LEAFY TWIG | 877L01IZ0P | ACTIB |
| PHOSPHORIC ACID | E4GA8884NN | ACTIB |
| TOXICODENDRON PUBESCENS LEAF | 6IO182RP7A | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg |
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 |
|---|---|---|---|---|---|---|
| 75d71207-90ce-4a73-961d-5bfe34e20daf | 15dfc9a0-b974-414f-bf06-4c508f9c413d | 2017-02-15 | Warnings | 15dfc9a0-b974-414f-bf06-4c508f9c413d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.