BONE HP
- Product NDC
- 43406-0611
- 11-digit product format
- 434060611
- Labeler code
- 43406
- Product ID
- 43406-0611_c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Borate, Oyster Shell Calcium Carbonate Crude, Calcium Fluoride, Tribasic Calcium Phosphate, Eupatorium Perfoliatum Flowering Top, Iron, Hydrofluoric Acid, Hekla Lava, Toxicodendron Pubescens Leaf, Ruta Graveolens Flowering Top, Silicon Dioxide, Comfrey Root.
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Natural Creations, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-06-01
- Substance
- CALCIUM FLUORIDE; COMFREY ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; HEKLA LAVA; HYDROFLUORIC ACID; IRON; OYSTER SHELL CALCIUM CARBONATE, CRUDE; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE; SODIUM BORATE; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATE
- Active strength
- 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BONE HP
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CALCIUM FLUORIDE | 30 [hp_C]/mL |
| COMFREY ROOT | 30 [hp_C]/mL |
| EUPATORIUM PERFOLIATUM FLOWERING TOP | 30 [hp_C]/mL |
| HEKLA LAVA | 30 [hp_C]/mL |
| HYDROFLUORIC ACID | 30 [hp_C]/mL |
| IRON | 30 [hp_C]/mL |
| OYSTER SHELL CALCIUM CARBONATE, CRUDE | 30 [hp_C]/mL |
| RUTA GRAVEOLENS FLOWERING TOP | 30 [hp_C]/mL |
| SILICON DIOXIDE | 30 [hp_C]/mL |
| SODIUM BORATE | 30 [hp_C]/mL |
| TOXICODENDRON PUBESCENS LEAF | 30 [hp_C]/mL |
| TRIBASIC CALCIUM PHOSPHATE | 30 [hp_C]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O3B55K4YKI, M9VVZ08EKQ, 1W0775VX6E, C21158IIRK, RGL5YE86CZ, E1UOL152H7, 2E32821G6I, N94C2U587S, ETJ7Z6XBU4, 91MBZ8H3QO, 6IO182RP7A, 91D9GV0Z28 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43406-0611-1 | BONE HP | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43406-0611 | BONE HP (SODIUM BORATE, OYSTER SHELL CALCIUM CARBONATE CRUDE, CALCIUM FLUORIDE, TRIBASIC CALCIUM PHOSPHATE, EUPATORIUM PERFOLIATUM FLOWERING TOP, IRON, HYDROFLUORIC ACID, HEKLA LAVA, TOXICODENDRON PUBESCENS LEAF, RUTA GRAVEOLENS FLOWERING TOP, SILICON DIOXIDE, COMFREY ROOT.) LIQUID [NATURAL CREATIONS, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20220304_93d2b385-9ce3-4d16-b428-1638e9a55f92.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43406-0611-1 | 43406061101 | 30 mL in 1 BOTTLE, DROPPER (43406-0611-1) | 30 ml | 2016-06-01 | 0000-00-00 | No | No | Current |