Thyrotox NDC 43857-0010

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0010Add 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
43857-0010-1	43857001001	30 mL in 1 BOTTLE, DROPPER (43857-0010-1)Marketed from Aug 10, 2016

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): Thyrotox
Generic name (nonproprietary): chondrus crispus, fucus vesiculosus, thyroidinum, belladonna, calcarea carbonica, conium maculatum, iodium, kali carbonicum, phosphorus, pulsatilla (vulgaris), silicea
Active ingredients: Chondrus crispus — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLSus scrofa thyroid — 8 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLIodine — 12 [hp_X]/mLPotassium carbonate — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPulsatilla vulgaris — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 16, 2013
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0010_33bc9bbd-68e3-461a-a96d-ce9773d8baf9SPL ID 33bc9bbd-68e3-461a-a96d-ce9773d8baf9SPL set ID e229a260-13f3-4136-b325-9a8954f8a327UNII OQS23HUA1X, 535G2ABX9M, 6RV024OAUQ, WQZ3G9PF0H, 2E32821G6I, Q28R5GF371, 9679TC07X4, BQN1B9B9HA, 27YLU75U4W, I76KB35JEV, ETJ7Z6XBU4

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

N443857001001 followed by a unit qualifier and the quantity

Package 43857-0010-01. 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 10, 2016.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of difficulty swallowing, flushed face, glaring eyes, excited mental state, nervous & excitable.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)