Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Thyropar NDC 44911-0683
Fucus vesiculosus 3 [hp_X]/mL + 12 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0683-1 | 44911068301 | 30 mL in 1 BOTTLE, DROPPER (44911-0683-1)Marketed from Oct 26, 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)
- Thyropar
- Generic name (nonproprietary)
- fucus vesiculosus, spongia tosta, glandula suprarenalis suis, hypophysis suis, thyroidinum (suis), bromium, calcarea carbonica, graphites, iodium, lachesis mutus, levothyroxinum, pulsatilla (pratensis), selenium metallicum
- Active ingredients
- Fucus vesiculosus — 3 [hp_X]/mLSpongia officinalis skeleton, Roasted — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLSus scrofa pituitary gland — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLBromine — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLLevothyroxine — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSelenium — 12 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Energique, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Thyroxine (Chemical structure)
- Identifiers
- Product ID 44911-0683_75a0cc2a-9284-413a-a91e-0c12a99594ecSPL ID 75a0cc2a-9284-413a-a91e-0c12a99594ecSPL set ID fe5065b4-7332-44fc-843a-f24b1e7a44e7UNII 535G2ABX9M, 1PIP394IID, 398IYQ16YV, L0PFEMQ1DT, 6RV024OAUQ, SBV4XY874G, 2E32821G6I, 4QQN74LH4O, 9679TC07X4, VSW71SS07I, Q51BO43MG4, 8E272251DI, H6241UJ22BUPC 0363113700398
- Pharmacologic class
- l-Thyroxine
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
N444911068301followed by a unit qualifier and the quantityPackage 44911-0683-01. 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)
USES: May temporarily relieve: • exhaustion and heaviness of the body • dry rough skin • dry cough • difficulty swallowing • swollen throat.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Excerpt only. Read the full label for complete information.
- openFDA data updated
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