Mycotox NDC 83027-0133

NDC codes

FDA NDC Directory

Product NDC (as listed)83027-0133Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83027-0133Add 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
83027-0133-1	83027013301	60 mL in 1 BOTTLE, SPRAY (83027-0133-1)Marketed from Sep 25, 2024

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): Mycotox
Generic name (nonproprietary): glandula suprarenalis (bovine), spleen (bovine), tabebuia impetiginosa (pau d arco), thuja occidentalis, thymus (ovine), thyroidinum (bovine), borax, colchicum autumnale, lacticum acidum, lymph node (suis), arsenicum album, zincum metallicum, aspergillus niger, candida albicans, candida parapsilosis, mucor racemosus, torula cerevisiae, alternaria tenuis nees, candida krusei, rhizopus nigricans, candida tropicalis
Active ingredients: Bos taurus adrenal gland — 6 [hp_X]/mLBos taurus spleen — 6 [hp_X]/mLHandroanthus impetiginosus bark — 6 [hp_X]/mLThuja occidentalis leafy twig — 6 [hp_X]/mLLamb — 6 [hp_X]/mLThyroid, Bovine — 6 [hp_X]/mLSodium borate — 6 [hp_X]/mLColchicum autumnale bulb — 6 [hp_X]/mLLactic acid, Dl- — 6 [hp_X]/mLSus scrofa lymph — 8 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLZinc — 12 [hp_X]/mLAspergillus niger var. Niger — 16 [hp_X]/mLCandida albicans — 16 [hp_X]/mLCandida parapsilosis — 16 [hp_X]/mLMucor racemosus — 16 [hp_X]/mLSaccharomyces cerevisiae — 16 [hp_X]/mLAlternaria alternata — 60 [hp_X]/mLIssatchenkia orientalis whole — 16 [hp_C]/mLRhizopus stolonifer — 16 [hp_C]/mLCandida tropicalis — 32 [hp_C]/mL
Dosage form: Spray
Route: Oral
Labeler: Nutritional Specialties, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 25, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)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 Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)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)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Meat Proteins (EXT)
Identifiers: Product ID 83027-0133_c2152d6c-9298-4238-9ed3-8b2719578a71SPL ID c2152d6c-9298-4238-9ed3-8b2719578a71SPL set ID f19eca09-6733-41e7-b0a9-94d5a3d8a728UNII M2776SWB29, 190Q9MB3U3, 6GLA1946WX, 1NT28V9397, FOF26T73HA, MN18OTN73W, 91MBZ8H3QO, 993QHL78E6, 3B8D35Y7S4, 33A7VYU29L, S7V92P67HO, J41CSQ7QDS, 9IOA40ANG6, 4D7G21HDBC, 0KZ676D44N, 17RH99LQ7G, 978D8U419H, 52B29REC7H, 138TJ2U1SD, FEE198DK4Q, Q222J2186WUPC 0649818024282
Pharmacologic class: Non-Standardized Food Allergenic Extract; 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

N483027013301 followed by a unit qualifier and the quantity

Package 83027-0133-01. 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 Aug 24, 2026.

Indications (excerpt from the label)

USES: Aids in temporary relief of achiness, fatigue, fever, headache, itchy eyes, red or itchy skin, rhinitis, and runny nose.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)