United States · FDA National Drug Code directory

BONE HP

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
43406-0611_c32b90a6-ddf7-41d9-b6f3-2d808a8d9b93
Product NDC
43406-0611
Form
LIQUID
Composition / generic term
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.
Labeler
Natural Creations, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20160601
Source listing expiry
20261231

Source-listed ingredients

  • 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

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 mL in 1 BOTTLE, DROPPER (43406-0611-1) · 43406-0611-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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