Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Thyrostat NDC 44911-0488
Fucus vesiculosus 3 [hp_X]/mL + 9 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0488-1 | 4491104880144911048801 | 30 mL in 1 BOTTLE, DROPPER (44911-0488-1)Marketed from Feb 22, 2019 |
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)
- Thyrostat
- Generic name (nonproprietary)
- fucus vesiculosus, spongia tosta, hypophysis suis, thyroidinum (suis), arsenicum iodatum, baryta carbonica, iodium, lycopus virginicus, natrum muriaticum
- Active ingredients
- Fucus vesiculosus — 3 [hp_X]/mLSpongia officinalis skeleton, Roasted — 3 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLArsenic triiodide — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLycopus virginicus — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Energique, Inc.NDC labeler code 44911
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 44911-0488_fddfa4f5-e354-49fc-ac87-1e2d94a592f2SPL ID fddfa4f5-e354-49fc-ac87-1e2d94a592f2SPL set ID 5c41b36c-e28f-4d60-b9b9-6b888d55ea95UNII 535G2ABX9M, 1PIP394IID, L0PFEMQ1DT, 6RV024OAUQ, 3029988O2T, 6P669D8HQ8, 2E32821G6I, 9679TC07X4, TWH5125Q6F, 451W47IQ8XUPC 0363113701401
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
N444911048801followed by a unit qualifier and the quantityPackage 44911-0488-01. 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 difficulty swallowing, flushed face, glaring eyes, excited mental state or nervousness.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.
About NDC 44911-0488
- What is NDC 44911-0488?
- 44911-0488 is the product NDC for Thyrostat, Fucus vesiculosus 3 [hp_X]/mL + 9 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Thyrostat (Fucus Vesiculosus, Spongia Tosta, Hypophysis Suis, Thyroidinum (Suis), Arsenicum Iodatum, Baryta Carbonica, Iodium, Lycopus Virginicus, Natrum Muriaticum).
- What is the active ingredient?
- Fucus vesiculosus, Spongia officinalis skeleton, Roasted, Sus scrofa pituitary gland, Thyroid, Arsenic triiodide, Barium carbonate, Oyster shell calcium carbonate, Crude, Iodine, Lycopus virginicus, Sodium chloride.
- Who is the labeler?
- Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Thyrostat?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.