Ring Relief NDC 17312-001

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-001Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0001Add 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
17312-001-15	17312000115	1 BOTTLE, DROPPER in 1 PACKAGE (17312-001-15) / 10 mL in 1 BOTTLE, DROPPERMarketed from May 5, 2015

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): Ring Relief
Generic name (nonproprietary): arnica montana, calcium sulfide, hypericum perforatum, lycopodium clavatum spore, thiosinaminum, mercurius solubilis, salicylic acid, silicon dioxide, allylthiourea
Active ingredients: Arnica montana — 6 [hp_X]/mLCalcium sulfide — 13 [hp_X]/mLHypericum perforatum — 6 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLMercurius solubilis — 13 [hp_X]/mLSalicylic acid — 6 [hp_X]/mLSilicon dioxide — 13 [hp_X]/mLAllylthiourea — 6 [hp_X]/mL
Dosage form: Liquid
Route: Auricular (Otic)
Labeler: TRP Company
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 1, 2006
Listing expires: Dec 31, 2026
Identifiers: Product ID 17312-001_46065bc3-19da-9699-e063-6394a90a386fSPL ID 46065bc3-19da-9699-e063-6394a90a386fSPL set ID 1c9c7944-31a9-4019-aad5-6b7f86084b53UNII O80TY208ZW, 1MBW07J51Q, XK4IUX8MNB, C88X29Y479, 324Y4038G2, O414PZ4LPZ, ETJ7Z6XBU4, 706IDJ14B7UPC 0858961001334

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N417312000115 followed by a unit qualifier and the quantity

Package 17312-0001-15. 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 Dec 15, 2025.

Indications (excerpt from the label)

Uses:* According to homeopathic indications, these ingredients temporarily relieve Tinnitus symptoms such as: • Ringing • Buzzing • Roaring • Nerve and Noise Sensitivity • Pounding • Discomfort • Wax buildup after serious causes have been ruled out by a physician. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)