Immuno Fortifier Liquid
NDC Package 43857-0454-1
Package Information
Immuno Fortifier (echinacea (angustifolia), hydrastis canadensis, ligusticum porteri, myrrha, nasturtium aquaticum, tabebuia impetiginosa, trigonella foenum-graecum, ascorbic acid, pinus sylvestris, lymph (suis), medulla ossis suis, spleen (suis), thymus (suis), hepar sulphuris calcareum, phosphoricum acidum, silicea) liquids is for temporary relief of painful sore throat, painful earache, and minor bronchial irritation with yellow expectoration. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0454.
Identification & Billing
Clinical Specifications
- ASCORBIC ACID 6 [hp_X]/mL
- CALCIUM SULFIDE 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
- FENUGREEK SEED 3 [hp_X]/mL
- GOLDENSEAL 5 [hp_X]/mL
- LIGUSTICUM PORTERI ROOT 3 [hp_X]/mL
- MYRRH 3 [hp_X]/mL
- NASTURTIUM OFFICINALE 3 [hp_X]/mL
- PHOSPHORIC ACID 12 [hp_X]/mL
- PINUS SYLVESTRIS LEAFY TWIG 6 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL
- SUS SCROFA BONE MARROW 8 [hp_X]/mL
- SUS SCROFA LYMPH 8 [hp_X]/mL
- SUS SCROFA SPLEEN 8 [hp_X]/mL
- SUS SCROFA THYMUS 8 [hp_X]/mL
- TABEBUIA IMPETIGINOSA BARK 3 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0454 - Immuno Fortifier
- 43857-0454-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0454 - Immuno Fortifier
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 43857-0454-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Immuno Fortifier, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains ascorbic acid; calcium sulfide; echinacea angustifolia; fenugreek seed; goldenseal; ligusticum porteri root; myrrh; nasturtium officinale; phosphoric acid; pinus sylvestris leafy twig; silicon dioxide; sus scrofa bone marrow; sus scrofa lymph; sus scrofa spleen; sus scrofa thymus; tabebuia impetiginosa bark 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 Bioactive Nutritional, Inc. on July 21, 2017. The current certification is valid through December 31, 2026.
How is this Bioactive Nutritional, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857045401. 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.