Home FDA labels c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93 BONE HP openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name BONE HP
Generic 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.
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID 93d2b385-9ce3-4d16-b428-1638e9a55f92
SPL ID c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93
Version 5
Effective date 2025-11-13
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:22 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name BONE HP openfda.brand_name generic 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. openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0611-1 openfda.package_ndc ndc product 43406-0611 openfda.product_ndc ndc11 package 43406061101 derived:openfda.package_ndc spl id c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93 id spl set id 93d2b385-9ce3-4d16-b428-1638e9a55f92 set_id unii O3B55K4YKI openfda.unii unii 91MBZ8H3QO openfda.unii unii 91D9GV0Z28 openfda.unii unii N94C2U587S openfda.unii unii ETJ7Z6XBU4 openfda.unii unii RGL5YE86CZ openfda.unii unii M9VVZ08EKQ openfda.unii unii 2E32821G6I openfda.unii unii 6IO182RP7A openfda.unii unii C21158IIRK openfda.unii unii E1UOL152H7 openfda.unii unii 1W0775VX6E openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: * Consult a physician for use in children under 12 years of age. * IF PREGNANT OR BREAST-FEEDING , ask a health care professional before use. * KEEP OUT OF THE REACH OF CHILDREN . In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. * Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.