Allerforce Liquid
NDC Package 43857-0016-1
Package Information
Allerforce (chondrus crispus, glycyrrhiza glabra, sarsaparilla, zingiber officinale, adrenalinum, allium cepa, aralia racemosa, arsenicum album, calcarea carbonica, cantharis, iodium, natrum carbonicum, rhus tox,) liquids is for temporary relief of hay fever, sinus congestion, bronchial irritation, itching of the eyelids, stuffy nose with headache, cough, hoarseness. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0016.
Identification & Billing
Clinical Specifications
- ARALIA RACEMOSA ROOT 12 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- CHONDRUS CRISPUS 3 [hp_X]/mL
- EPINEPHRINE 8 [hp_X]/mL
- GINGER 3 [hp_X]/mL
- GLYCYRRHIZA GLABRA 3 [hp_X]/mL
- IODINE 12 [hp_X]/mL
- LYTTA VESICATORIA 12 [hp_X]/mL
- ONION 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
- SMILAX ORNATA ROOT 3 [hp_X]/mL
- SODIUM CARBONATE 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Allergens - [CS]
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Food Additives - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Vegetable Proteins - [CS]
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 43857 - Bioactive Nutritional, Inc.
- 43857-0016 - Allerforce
- 43857-0016-1 - 30 mL in 1 BOTTLE, DROPPER
- 43857-0016 - Allerforce
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 43857-0016-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Allerforce, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains aralia racemosa root; arsenic trioxide; chondrus crispus; epinephrine; ginger; glycyrrhiza glabra; iodine; lytta vesicatoria; onion; oyster shell calcium carbonate, crude; smilax ornata root; sodium carbonate; 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 Bioactive Nutritional, Inc. on February 19, 2013. 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: 43857001601. 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.