Additivestat Liquid
NDC Package 44911-0630-1
Package Information
Additivestat (trifolium pratense, petroleum, phytolacca decandra, arsenicum album, chelidonium majus, lycopodium clavatum, nux vomica, phosphoricum acidum, phosphorus, nitricum acidum) liquids May temporarily relieve debility, exhaustion after slight exertion, and nausea.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0630.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- CHELIDONIUM MAJUS WHOLE 12 [hp_X]/mL
- KEROSENE 6 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- NITRIC ACID 12 [hp_X]/mL
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0630 - Additivestat
- 44911-0630-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0630 - Additivestat
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 44911-0630-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Additivestat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arsenic trioxide; chelidonium majus whole; kerosene; lycopodium clavatum spore; nitric acid; phosphoric acid; phosphorus; phytolacca americana root; strychnos nux-vomica seed; trifolium pratense flower 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 Energique, Inc. on December 30, 2020. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911063001. 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.