Chemtox NDC 43857-0546

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0546Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0546Add 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
43857-0546-1	43857054601	30 mL in 1 BOTTLE, DROPPER (43857-0546-1)Marketed from Dec 26, 2019

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): Chemtox
Generic name (nonproprietary): triticum aestivum, berberis vulgaris, glycyrrhiza glabra, lappa major, rhamnus frangula, rhamnus purshiana, stillingia sylvatica, trifolium pratense, xanthoxylum fraxineum, phytolacca decandra, glandula suprarenalis suis, hepar suis, lymph node (suis), thyroidinum (suis), belladonna, lycopodium clavatum, nitricum acidum, nux vomica, phosphoricum acidum, phosphorus, salicylicum acidum, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum, chlorinum, potassium sorbate,
Active ingredients: Triticum aestivum whole — 1 [hp_X]/mLBerberis vulgaris root bark — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLFrangula alnus bark — 3 [hp_X]/mLFrangula purshiana bark — 3 [hp_X]/mLStillingia sylvatica root — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLZanthoxylum americanum bark — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLSus scrofa adrenal gland — 8 [hp_X]/mLPork liver — 8 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLAtropa belladonna whole — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSalicylic acid — 30 [hp_X]/mLCortisone acetate — 30 [hp_X]/mLEugenol — 30 [hp_X]/mLStearyl alcohol — 30 [hp_X]/mLXylitol — 30 [hp_X]/mLEstrone — 30 [hp_X]/mLBenzoic acid — 30 [hp_X]/mLChlorine — 30 [hp_X]/mLPotassium sorbate — 30 [hp_X]/mLSorbitol — 30 [hp_X]/mLResorcinol — 30 [hp_X]/mLBenzyl alcohol — 30 [hp_X]/mLLactic acid, Dl- — 30 [hp_X]/mLIsopropyl palmitate — 30 [hp_X]/mLBoric acid — 30 [hp_X]/mLAcetic acid — 30 [hp_X]/mLPhenylbutazone — 30 [hp_X]/mLPetrolatum — 30 [hp_X]/mLLead — 30 [hp_X]/mLCorticotropin — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 26, 2019
Marketing end: Jun 7, 2028
Other FDA classes: Adrenocorticotropic Hormone (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)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 43857-0546_b883884e-2c8e-4cd1-b68b-331639cb0e4aSPL ID b883884e-2c8e-4cd1-b68b-331639cb0e4aSPL set ID 9aa060f1-f8f6-46e6-a7d0-bd46a73f2676UNII 3C3Y389JBU, 1TH8Q20J0U, 2788Z9758H, 597E9BI3Z3, S2D77IH61R, 4VBP01X99F, QBR70R4FBK, 4JS0838828, A4KL1HMZ7T, 11E6VI8VEG, 398IYQ16YV, 6EC706HI7F, 33A7VYU29L, 6RV024OAUQ, DSV74G1P2J, C88X29Y479, 411VRN1TV4, 269XH13919, E4GA8884NN, 27YLU75U4W, O414PZ4LPZ, 883WKN7W8X, 3T8H1794QW, 2KR89I4H1Y, VCQ006KQ1E, 2DI9HA706A, 8SKN0B0MIM, 4R7X1O2820, 1VPU26JZZ4, 506T60A25R, YUL4LO94HK, LKG8494WBH, 3B8D35Y7S4, 8CRQ2TH63M, R57ZHV85D4, Q40Q9N063P, GN5P7K3T8S, 4T6H12BN9U, 2P299V784P, K0U68Q2TXA
Pharmacologic class: Adrenocorticotropic Hormone; Corticosteroid; Nitrogen Binding Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Pediculicide; 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

N443857054601 followed by a unit qualifier and the quantity

Package 43857-0546-01. 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 Oct 17, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of weakness & exhaustion, minor abdominal cramps & bloating, and vomiting.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)