Anxiety Ii Hp Liquid
NDC Package 43406-0004-1
Package Information
Anxiety Ii Hp (aconitum napellus, arsenic trioxide, atropa belladonna, oyster shell calcium carbonate, crude, activated charcoal, human breast tumor cell, causticum, gelsemium sempervirens root, lachesis muta venom, mercury, sodium chloride, nitric acid, phosphorus, toxicodendron pubescens leaf) liquids is uSES: Temporarily relieves anxieties, worries, fears, and/or oversensitive feelings. This formulation utilizes a liquid delivery system. Marketed by Natural Creations, Inc., this product is identified by NDC 43406-0004.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS WHOLE 30 [hp_C]/mL
- ACTIVATED CHARCOAL 30 [hp_C]/mL
- ARSENIC TRIOXIDE 30 [hp_C]/mL
- ATROPA BELLADONNA 30 [hp_C]/mL
- CAUSTICUM 30 [hp_C]/mL
- GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/mL
- HUMAN BREAST TUMOR CELL 30 [hp_C]/mL
- LACHESIS MUTA VENOM 30 [hp_C]/mL
- MERCURY 30 [hp_C]/mL
- NITRIC ACID 30 [hp_C]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
- PHOSPHORUS 30 [hp_C]/mL
- SODIUM CHLORIDE 30 [hp_C]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL
Regulatory & Marketing
Hierarchy Structure
- 43406 - Natural Creations, Inc.
- 43406-0004 - Anxiety Ii Hp
- 43406-0004-1 - 30 mL in 1 BOTTLE, DROPPER
- 43406-0004 - Anxiety Ii 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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 43406-0004-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Anxiety Ii Hp, a human over the counter drug labeled by Natural Creations, Inc.. This liquid is formulated for oral use and contains aconitum napellus whole; activated charcoal; arsenic trioxide; atropa belladonna; causticum; gelsemium sempervirens root; human breast tumor cell; lachesis muta venom; mercury; nitric acid; oyster shell calcium carbonate, crude; phosphorus; sodium chloride; toxicodendron pubescens leaf 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 May 29, 2007. 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: 43406000401. 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.