Tinnitus Relief NDC 61727-315

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-315Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0315Add 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
61727-315-21	61727031521	4 g in 1 TUBE (61727-315-21)Marketed from Jul 24, 2012

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Tinnitus Relief
Generic name (nonproprietary): cinchona officinalis bark,salicylic acid,quinine sulfate,ferrum phosphoricum,potassium chloride,calomel,allylthiourea,.
Active ingredients: Cinchona officinalis bark — 9 [hp_C]/4gSalicylic acid — 15 [hp_C]/4gQuinine sulfate — 9 [hp_C]/4gFerrum phosphoricum — 4 [hp_C]/4gPotassium chloride — 4 [hp_C]/4gCalomel — 4 [hp_C]/4gAllylthiourea — 4 [hp_C]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 24, 2012
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 61727-315_82fbfc25-3f57-460f-e053-2991aa0aad29SPL ID 82fbfc25-3f57-460f-e053-2991aa0aad29SPL set ID 30d67273-b9ec-4f3e-ace6-87a68325aaf1UNII S003A158SB, O414PZ4LPZ, KF7Z0E0Q2B, 91GQH8I5F7, 660YQ98I10, J2D46N657D, 706IDJ14B7UPC 0361727315212
Pharmacologic class: Antimalarial; Osmotic Laxative; Potassium Salt

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461727031521 followed by a unit qualifier and the quantity

Package 61727-0315-21. 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 Feb 28, 2019.

Indications (excerpt from the label)

Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)