Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Mytox NDC 83027-0092
Sodium borate 4 [hp_X]/mL + 6 more ingredients · Spray · Oral · Nutritional Specialties, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83027-0092-1 | 83027009201 | 60 mL in 1 BOTTLE, SPRAY (83027-0092-1)Marketed from Aug 2, 2023 |
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)
- Mytox
- Generic name (nonproprietary)
- borax, colchicum autumnale, drosera (rotundifolia), arsenicum album, ubidecarenonum, agaricus muscarius, bufo rana
- Active ingredients
- Sodium borate — 4 [hp_X]/mLColchicum autumnale bulb — 4 [hp_X]/mLDrosera rotundifolia whole — 6 [hp_X]/mLArsenic trioxide — 8 [hp_X]/mLUbidecarenone — 8 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLBufo bufo cutaneous gland — 12 [hp_X]/mL
- Dosage form
- Spray
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 83027-0092_9b5cf627-6fce-485d-8a4c-dd1d6f32fe0fSPL ID 9b5cf627-6fce-485d-8a4c-dd1d6f32fe0fSPL set ID 72563dce-17ea-49da-be13-122543af7623UNII 91MBZ8H3QO, 993QHL78E6, QR44N9XPJQ, S7V92P67HO, EJ27X76M46, DIF093I037, Q59QU6N72QUPC 0649818024213
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
N483027009201followed by a unit qualifier and the quantityPackage 83027-0092-01. 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 .
Indications (excerpt from the label)
INDICATIONS: Aids in temporary relief of symptoms associated with fungal conditions, such as night sweats, headache, fatigue, muscle aches, joint pain, and itchy, red or scaly skin† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.