Bone Hp Liquid
NDC Package 43406-0611-1
Package Information
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.) liquids is USES: Temporarily relieves bone aches and pains.**. This formulation utilizes a liquid delivery system. Marketed by Natural Creations, Inc., this product is identified by NDC 43406-0611.
Identification & Billing
Clinical Specifications
- 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
Regulatory & Marketing
Hierarchy Structure
- 43406 - Natural Creations, Inc.
- 43406-0611 - Bone Hp
- 43406-0611-1 - 30 mL in 1 BOTTLE, DROPPER
- 43406-0611 - Bone Hp
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43406-0611-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Bone Hp, a human over the counter drug labeled by Natural Creations, Inc.. This liquid is formulated for oral use and contains 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 as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Natural Creations, Inc. on June 01, 2016. The current certification is valid through December 31, 2026.
How is this Natural Creations, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43406061101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.