Oligo Bio Iodine NDC 43857-0541

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0541Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0541Add 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
43857-0541-1	43857054101	30 mL in 1 BOTTLE, DROPPER (43857-0541-1)Marketed from Nov 21, 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): Oligo Bio Iodine
Generic name (nonproprietary): chelidonium majus, iodium, lycopus virginicus, ginkgo biloba, pinus sylvestris, fucus vesiculosus, spongia tosta, germanium sesquioxide, hypophysis suis, thyroidinum (suis), cysteinum, manganese gluconate, alpha-ketoglutaricum acidum, calcarea carbonica, ferrum iodatum, fumaricum acidum, kali iodatum, natrum oxalaceticum, pulsatilla (vulgaris), argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum metallicum, niccolum metallicum,
Active ingredients: Chelidonium majus whole — 3 [hp_X]/mLIodine — 4 [hp_X]/mLLycopus virginicus whole — 4 [hp_X]/mLGinkgo — 6 [hp_X]/mLPinus sylvestris leafy twig — 6 [hp_X]/mLFucus vesiculosus — 6 [hp_X]/mLSpongia officinalis skeleton, Roasted — 7 [hp_X]/mLGermanium sesquioxide — 8 [hp_X]/mLSus scrofa pituitary gland — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLCysteine — 9 [hp_X]/mLManganese gluconate — 10 [hp_X]/mLOxogluric acid — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLFerrous iodide — 12 [hp_X]/mLFumaric acid — 12 [hp_X]/mLPotassium iodide — 12 [hp_X]/mLSodium diethyl oxalacetate — 12 [hp_X]/mLPulsatilla vulgaris whole — 12 [hp_X]/mLSilver — 12 [hp_X]/mLGold — 12 [hp_X]/mLCopper — 12 [hp_X]/mLEugenol — 12 [hp_X]/mLFormaldehyde — 12 [hp_X]/mLLidocaine — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLMolybdenum — 12 [hp_X]/mLNickel — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLTin — 12 [hp_X]/mLTitanium — 12 [hp_X]/mLZinc — 12 [hp_X]/mLRubella virus — 16 [hp_X]/mLMumps virus — 30 [hp_X]/mLHuman coxsackievirus a2 — 16 [hp_C]/mLHuman coxsackievirus a7 — 16 [hp_C]/mLHuman coxsackievirus b1 — 16 [hp_C]/mLHuman coxsackievirus b3 — 16 [hp_C]/mLHuman coxsackievirus b4 — 16 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 21, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Amides (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)Local Anesthesia (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 43857-0541_7042f927-8a49-48aa-a0d6-5132f25fcd0eSPL ID 7042f927-8a49-48aa-a0d6-5132f25fcd0eSPL set ID 90e3028e-9e1e-4887-8b7c-f712bf67cd52UNII 7E889U5RNN, 9679TC07X4, TWH5125Q6F, 19FUJ2C58T, Q1RGP4UB73, 535G2ABX9M, 1PIP394IID, 96WE91N25T, L0PFEMQ1DT, 6RV024OAUQ, K848JZ4886, 9YY2F980SV, 8ID597Z82X, 2E32821G6I, F5452U54PN, 88XHZ13131, 1C4QK22F9J, 6CA025Y4FG, I76KB35JEV, 3M4G523W1G, 79Y1949PYO, 789U1901C5, 3T8H1794QW, 1HG84L3525, 98PI200987, 324Y4038G2, 81AH48963U, 7OV03QG267, 5TWQ1V240M, 387GMG9FH5, D1JT611TNE, J41CSQ7QDS, U751HEX436, YF0S03R447, 82KK5J435E, P3026TK92O, ADL68M27WD, 69O1DAO10G, FYF75V7FDY
Pharmacologic class: Amide Local Anesthetic; Antiarrhythmic; Copper-containing Intrauterine Device; Paramagnetic Contrast 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

N443857054101 followed by a unit qualifier and the quantity

Package 43857-0541-01. 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 Nov 7, 2023.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of fatigue, muscular weakness, weak pulse, tendency to faint, cold hands & feet, low blood pressure, nervous tremor of limbs & sensitive to cold.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)