What is NDC 17312-023?

17312-023 is the product NDC for Ring Relief, Arnica montana 6 [hp_X]/1 + 7 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Ring Relief (Arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea -).

What is the active ingredient?

Arnica montana, Calcium sulfide, Hypericum perforatum, Lycopodium clavatum spore, Mercurius solubilis, Salicylic acid, Silicon dioxide, Allylthiourea.

TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ring Relief?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ring Relief NDC 17312-023 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-023Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0023Add 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
17312-023-14	1731200231417312002314	1 BOTTLE in 1 PACKAGE (17312-023-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLEMarketed from Dec 1, 2011

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 - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea -
Active ingredients: Arnica montana — 6 [hp_X]/1Calcium sulfide — 13 [hp_X]/1Hypericum perforatum — 6 [hp_X]/1Lycopodium clavatum spore — 12 [hp_X]/1Mercurius solubilis — 13 [hp_X]/1Salicylic acid — 6 [hp_X]/1Silicon dioxide — 13 [hp_X]/1Allylthiourea — 6 [hp_X]/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 17312-023_4606551b-3bef-8c1b-e063-6394a90a0160SPL ID 4606551b-3bef-8c1b-e063-6394a90a0160SPL set ID aa2cd967-3c27-4afe-8751-7ea50ab62913UNII O80TY208ZW, 1MBW07J51Q, XK4IUX8MNB, C88X29Y479, 324Y4038G2, O414PZ4LPZ, ETJ7Z6XBU4, 706IDJ14B7UPC 0858961001150

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

N417312002314 followed by a unit qualifier and the quantity

Package 17312-0023-14. 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)

About NDC 17312-023

What is NDC 17312-023?: 17312-023 is the product NDC for Ring Relief, Arnica montana 6 [hp_X]/1 + 7 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ring Relief (Arnica montana - calcium sulfide - hypericum perforatum - lycopodium clavatum spore - mercurius solubilis - salicylic acid - silicon dioxide - allylthiourea -).
What is the active ingredient?: Arnica montana, Calcium sulfide, Hypericum perforatum, Lycopodium clavatum spore, Mercurius solubilis, Salicylic acid, Silicon dioxide, Allylthiourea.
Who is the labeler?: TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ring Relief?: 1 other product NDC are listed under this name. See all Ring Relief NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ring Relief NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ring Reliefarnica montana, calcium sulfide, hypericum perforatum, lycopodium clavatum spore, thiosinaminum, mercurius solubilis, salicylic acid, silicon dioxide, allylthiourea	Arnica montana 6 [hp_X]/mL + 7 more ingredients	LiquidAuricular (Otic)	TRP Company	17312-001	17312-0001-15