Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Pyostat NDC 44911-0709
Baptisia tinctoria root 3 [hp_X]/mL + 9 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0709-1 | 44911070901 | 60 mL in 1 BOTTLE, DROPPER (44911-0709-1)Marketed from Apr 18, 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)
- Pyostat
- Generic name (nonproprietary)
- baptisia tinctoria, echinacea (angustifolia), arsenicum album, belladonna, crotalus horridus, hyoscyamus niger, lachesis mutus, pyrogenium, tarentula cubensis, anthracinum
- Active ingredients
- Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLCrotalus horridus horridus venom — 12 [hp_X]/mLHyoscyamus niger — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLRancid beef — 12 [hp_X]/mLCitharacanthus spinicrus — 12 [hp_X]/mLBacillus anthracis immunoserum rabbit — 30 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Energique, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Marketing end
- Identifiers
- Product ID 44911-0709_de9c9cf5-3f40-4936-a95d-1a88e80e8300SPL ID de9c9cf5-3f40-4936-a95d-1a88e80e8300SPL set ID 427417ce-72a8-4d46-be24-b8b0fdc85458UNII 5EF0HWI5WU, VB06AV5US8, S7V92P67HO, WQZ3G9PF0H, YHA2XLJ956, 4WRK2153H3, VSW71SS07I, 29SUH5R3HU, 3Y5X6RT823, 41LZ22DD4NUPC 0363113701029
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
N444911070901followed by a unit qualifier and the quantityPackage 44911-0709-01. 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: May temporarily relieve redness, swelling, pus, offensive discharges, fever, muscular soreness, swollen lymph nodes, and burning/stinging pain, bites, and wounds.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.