Home NDC 43406-0611 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 SODIUM BORATE 30 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL CALCIUM FLUORIDE 30 [hp_C]/mL TRIBASIC CALCIUM PHOSPHATE 30 [hp_C]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP 30 [hp_C]/mL IRON 30 [hp_C]/mL HYDROFLUORIC ACID 30 [hp_C]/mL HEKLA LAVA 30 [hp_C]/mL TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL RUTA GRAVEOLENS FLOWERING TOP 30 [hp_C]/mL SILICON DIOXIDE 30 [hp_C]/mL COMFREY ROOT 30 [hp_C]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 12 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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
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 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. Natural Creations, Inc. 93d2b385-9ce3-4d16-b428-1638e9a55f92 2025-11-13 Warnings Exact identifier ndc (product): 43406-0611
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