Micox NDC 17089-420

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-420Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0420Add 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
17089-420-18	17089042018	1 BOTTLE, DROPPER in 1 BOX (17089-420-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Dec 21, 2018

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Micox
Generic name (nonproprietary): aspergillus niger var. niger - candida albicans - centella asiatica - malic acid - mercuric chloride - rhizopus stolonifer - sodium diethyl oxalacetate - sulfur - tabebuia impetiginosa bark -
Active ingredients: Aspergillus niger var. Niger — 30 [hp_X]/30mLCandida albicans — 30 [hp_X]/30mLMalic acid — 12 [hp_X]/30mLCentella asiatica — 6 [hp_X]/30mLMercuric chloride — 6 [hp_X]/30mLRhizopus stolonifer — 30 [hp_X]/30mLSodium diethyl oxalacetate — 12 [hp_X]/30mLTabebuia impetiginosa bark — 4 [hp_X]/30mLSulfur — 6 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spa
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 27, 2010
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 17089-420_53f56dc9-eac1-51a5-e063-6394a90a896fSPL ID 53f56dc9-eac1-51a5-e063-6394a90a896fSPL set ID 790b50d3-8e1e-4c36-be74-f30c51ca7895UNII 9IOA40ANG6, 4D7G21HDBC, 817L1N4CKP, 7M867G6T1U, 53GH7MZT1R, FEE198DK4Q, 6CA025Y4FG, 6GLA1946WX, 70FD1KFU70
Pharmacologic class: Non-Standardized Fungal Allergenic Extract

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

N417089042018 followed by a unit qualifier and the quantity

Package 17089-0420-18. 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 Jun 11, 2026.

Indications (excerpt from the label)

Take 15 minutes before meals.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)