Additox NDC 43857-0487

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0487Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0487Add 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
43857-0487-1	43857048701	30 mL in 1 BOTTLE, DROPPER (43857-0487-1)Marketed from Jul 18, 2018

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): Additox
Generic name (nonproprietary): trifolium pratense, xanthoxylum fraxineum, phytolacca decandra, arsenicum album, belladonna, chelidonium majus, lycopodium clavatum, phosphoricum acidum, aspartame, benzalkonium chloride, formalinum, methylene chloride, methylparaben, propylparaben, sodium benzoate, sodium citrate, titanium dioxide, zincum oxydatum
Active ingredients: Trifolium pratense flower — 3 [hp_X]/mLZanthoxylum americanum bark — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLChelidonium majus — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLAspartame — 30 [hp_X]/mLBenzalkonium chloride — 30 [hp_X]/mLFormaldehyde — 30 [hp_X]/mLMethylene chloride — 30 [hp_X]/mLMethylparaben — 30 [hp_X]/mLPropylparaben — 30 [hp_X]/mLSodium benzoate — 30 [hp_X]/mLSodium citrate — 30 [hp_X]/mLTitanium dioxide — 30 [hp_X]/mLZinc oxide — 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: Jul 18, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 43857-0487_e095c202-fcfe-4cc8-8985-4e6c3a0f35b0SPL ID e095c202-fcfe-4cc8-8985-4e6c3a0f35b0SPL set ID 319ee2fe-58e3-495e-bf0d-df201f6fbb1cUNII 4JS0838828, A4KL1HMZ7T, 11E6VI8VEG, S7V92P67HO, WQZ3G9PF0H, 7E889U5RNN, C88X29Y479, E4GA8884NN, Z0H242BBR1, F5UM2KM3W7, 1HG84L3525, 588X2YUY0A, A2I8C7HI9T, Z8IX2SC1OH, OJ245FE5EU, 1Q73Q2JULR, 15FIX9V2JP, SOI2LOH54Z
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Copper Absorption Inhibitor; Nitrogen Binding Agent; 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

N443857048701 followed by a unit qualifier and the quantity

Package 43857-0487-01. 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 Jul 18, 2018.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of debility, exhaustion, exhaustion after slight exertion, and dysentery.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)