Neurotox NDC 43857-0632

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0632Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0632Add 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
43857-0632-1	43857063201	60 mL in 1 BOTTLE, DROPPER (43857-0632-1)Marketed from Aug 9, 2023

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): Neurotox
Generic name (nonproprietary): agaricus muscarius, coccus cacti, conium maculatum, lycopodium clavatum, phosphorus, aluminium metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium, cadmium metallicum, cerium metallicum, cesium chloride, chromium, cobaltum metallicum, cuprum metallicum, dysprosium metallicum, erbium metallicum, europium metallicum, ferrum metallicum, gadolinium metallicum, germanium sesquioxide,
Active ingredients: Amanita muscaria fruiting body — 12 [hp_X]/mLProtortonia cacti — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLAluminum — 12 [hp_X]/mLAntimony trisulfide — 12 [hp_X]/mLSilver — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLGold — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBeryllium — 12 [hp_X]/mLBismuth — 12 [hp_X]/mLBoron — 12 [hp_X]/mLBromine — 12 [hp_X]/mLCadmium — 12 [hp_X]/mLCerium — 12 [hp_X]/mLCesium chloride — 12 [hp_X]/mLChromium — 12 [hp_X]/mLCobalt — 12 [hp_X]/mLCopper — 12 [hp_X]/mLDysprosium — 12 [hp_X]/mLErbium — 12 [hp_X]/mLEuropium — 12 [hp_X]/mLIron — 12 [hp_X]/mLGadolinium — 12 [hp_X]/mLGermanium sesquioxide — 12 [hp_X]/mLHolmium — 12 [hp_X]/mLIndium — 12 [hp_X]/mLLithium carbonate — 12 [hp_X]/mLMagnesium — 12 [hp_X]/mLManganese — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLMolybdenum — 12 [hp_X]/mLNeodymium oxide — 12 [hp_X]/mLNickel — 12 [hp_X]/mLOsmium — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLPlatinum — 12 [hp_X]/mLLead — 12 [hp_X]/mLPraseodymium — 12 [hp_X]/mLRhodium — 12 [hp_X]/mLRubidium nitrite — 12 [hp_X]/mLSamarium — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLTin — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mLTerbium — 12 [hp_X]/mLThallium — 12 [hp_X]/mLUranyl nitrate hexahydrate — 12 [hp_X]/mLVanadium — 12 [hp_X]/mLYtterbium oxide — 12 [hp_X]/mLZinc — 12 [hp_X]/mLGelsemium sempervirens root — 30 [hp_X]/mLInfluenza a virus a/victoria/2570/2019 ivr-215 (H1n1) antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLInfluenza a virus a/darwin/9/2021 ivr-228 (H3n2) antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLInfluenza b virus b/austria/1359417/2021 bvr-26 antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLInfluenza b virus b/phuket/3073/2013 antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLLatrodectus mactans — 30 [hp_X]/mLMeasles virus — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLCitharacanthus spinicrus — 30 [hp_X]/mLBotulinum toxin type a — 30 [hp_X]/mLEscherichia coli — 30 [hp_X]/mLProteus vulgaris — 30 [hp_X]/mLPseudomonas aeruginosa — 30 [hp_X]/mLProteus morganii — 30 [hp_X]/mLSalmonella enterica subsp. Enterica serovar typhi — 33 [hp_X]/mLLanthanum — 14 [hp_C]/mLClostridium perfringens — 15 [hp_C]/mLHuman herpesvirus 4 — 30 [hp_C]/mLNiobium — 30 [hp_C]/mLPoliovirus — 30 [hp_C]/mLTantalum — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 9, 2023
Marketing end: May 25, 2028
Other FDA classes: Acetylcholine Release Inhibitors (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Neuromuscular Blockade (Physiologic effect)
Identifiers: Product ID 43857-0632_28bfacec-d5ea-4620-86c1-76c2d6200295SPL ID 28bfacec-d5ea-4620-86c1-76c2d6200295SPL set ID 07a457c0-df0d-468a-b0d8-84c739c17b70UNII DIF093I037, LZB7TFX1LT, Q28R5GF371, C88X29Y479, 27YLU75U4W, CPD4NFA903, F79059A38U, 3M4G523W1G, S7V92P67HO, 79Y1949PYO, 6P669D8HQ8, OW5102UV6N, U015TT5I8H, N9E3X5056Q, SBV4XY874G, 00BH33GNGH, 30K4522N6T, GNR9HML8BA, 0R0008Q3JB, 3G0H8C9362, 789U1901C5, 1D4N45714Q, 77B218D3YE, 444W947O8O, E1UOL152H7, AU0V1LM3JT, 96WE91N25T, W1XX32SQN1, 045A6V3VFX, 2BMD2GNA4V, I38ZP9992A, 42Z2K6ZL8P, 324Y4038G2, 81AH48963U, AYT3H319PN, 7OV03QG267, 2E7M255OPY, 5TWQ1V240M, 49DFR088MY, 2P299V784P, NKN7EZA750, DMK383DSAC, 93722E7JA1, 42OD65L39F, H6241UJ22B, 387GMG9FH5, 41YPU4MMCA, 06SSF7P179, AD84R52XLF, 3V057702FY, 00J9J9XKDE, T66CZ53RP4, J41CSQ7QDS, 639KR60Q1Q, 34C49NV47P, P483J7GX6D, TBV2PPG6EF, H2198F8ZNA, XJJ7QA858R, HT3R7C012Q, 6IO182RP7A, 3Y5X6RT823, E211KPY694, 514B9K0L10, 11T9HCO30O, Y793W5V55N, 56X6LID5ZY, 760T5R8B3O, 6I3K30563S, OVP6XX033E, 2A26YW7PNX, 05175J654G, FZJ641678T, 6424HBN274
Pharmacologic class: Acetylcholine Release Inhibitor; Copper-containing Intrauterine Device; Mood Stabilizer; Neuromuscular Blocker; Standardized Chemical Allergen

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

N443857063201 followed by a unit qualifier and the quantity

Package 43857-0632-01. 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

Current FDA label (SPL), effective May 19, 2025.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of symptoms due to numbness, tingling, muscle cramps, and nerve pain.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)