Imucode NDC 43406-0685

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0685Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0685Add 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
43406-0685-1	43406068501	30 mL in 1 BOTTLE, DROPPER (43406-0685-1)Marketed from Jun 13, 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): Imucode
Generic name (nonproprietary): astragalus, hydrastis, adrenalinum, thyroidinum, pituitarum posterium, arsenicum alb, baptisia, baryta carb, baryta mur, bromium, candida alb, ceanothus, chininum sulph, conium, hepar sulph calc, ignatia, indium, iodium, merc solub, phytolacca, sulphur
Active ingredients: Goldenseal — 8 [hp_X]/mLEpinephrine — 9 [hp_X]/mLThyroid — 9 [hp_X]/mLSus scrofa pituitary gland, Posterior — 9 [hp_X]/mLAstragalus nuttallii leaf — 12 [hp_X]/mLBaptisia tinctoria whole — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBarium chloride dihydrate — 12 [hp_X]/mLBromine — 12 [hp_X]/mLCeanothus americanus leaf — 12 [hp_X]/mLQuinine sulfate — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLIndium — 12 [hp_X]/mLIodine — 12 [hp_X]/mLPhytolacca americana root — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLArsenic trioxide — 30 [hp_C]/mLCandida albicans — 30 [hp_C]/mLMercurius solubilis — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 13, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43406-0685_3d04e729-a756-4fd0-a848-a76b7d70f5f9SPL ID 3d04e729-a756-4fd0-a848-a76b7d70f5f9SPL set ID be30901c-0673-4af0-8128-83ed59ff04b1UNII ZW3Z11D0JV, YKH834O4BH, 6RV024OAUQ, E8S87O660T, NC1P15G4KZ, 5K1UO2888Y, 6P669D8HQ8, EL5GJ3U77E, SBV4XY874G, 25B1Y14T8N, KF7Z0E0Q2B, Q28R5GF371, 1MBW07J51Q, 1NM3M2487K, 045A6V3VFX, 9679TC07X4, 11E6VI8VEG, 70FD1KFU70, S7V92P67HO, 4D7G21HDBC, 324Y4038G2UPC 0877730001634
Pharmacologic class: Antimalarial; Catecholamine; Non-Standardized Fungal 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

N443406068501 followed by a unit qualifier and the quantity

Package 43406-0685-01. 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 Dec 21, 2018.

Indications (excerpt from the label)

USES: Temporarily relieves fever, aches & pains.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)