Adrenal Tonic NDC 43857-0057

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0057Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0057Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43857-0057-1	43857005701	60 mL in 1 BOTTLE, DROPPER (43857-0057-1)Marketed from May 23, 2016

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Adrenal Tonic
Generic name (nonproprietary): aralia quinquefolia, glycyrrhiza glabra, sarsaparilla, avena sativa, glandula suprarenalis bovine, adrenalinum, arsenicum album, kali phosphoricum, natrum muriaticum, nux vomica, phosphoricum acidum, veratrum album
Active ingredients: American ginseng — 1 [hp_X]/mLGlycyrrhiza glabra — 1 [hp_X]/mLSmilax ornata root — 1 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLBos taurus adrenal gland — 8 [hp_X]/mLEpinephrine — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLPotassium phosphate, Dibasic — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLVeratrum album root — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 23, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43857-0057_f59b92f7-2eea-41ea-ae7b-0efde6b7b25eSPL ID f59b92f7-2eea-41ea-ae7b-0efde6b7b25eSPL set ID 2bbf65e2-47b9-46d3-a8de-69bc543783f8UNII 8W75VCV53Q, 2788Z9758H, 2H1576D5WG, MA9CQJ3F7F, M2776SWB29, YKH834O4BH, S7V92P67HO, CI71S98N1Z, 451W47IQ8X, 269XH13919, E4GA8884NN, QNS6W5US1ZUPC 0810184340379
Pharmacologic class: Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443857005701 followed by a unit qualifier and the quantity

Package 43857-0057-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

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