What is NDC 17312-175?

17312-175 is the product NDC for Ring Relief PM Nighttime Formula, Arnica montana 6 [hp_X]/mL + 9 more ingredients liquid, 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 PM Nighttime Formula (Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea).

What is the active ingredient?

Arnica montana, Calcium sulfide, Hypericum perforatum, Lycopodium clavatum spore, Matricaria chamomilla, Salicylic acid, Silicon dioxide, Valerian, Allylthiourea, Passiflora incarnata flower.

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 PM Nighttime Formula?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ring Relief PM Nighttime Formula NDC 17312-175

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-175Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0175Add 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
17312-175-15	1731201751517312017515	1 BOTTLE, DROPPER in 1 PACKAGE (17312-175-15) / 10 mL in 1 BOTTLE, DROPPERMarketed from Sep 19, 2019

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 PM Nighttime Formula
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]/mLMatricaria chamomilla — 12 [hp_X]/mLSalicylic acid — 6 [hp_X]/mLSilicon dioxide — 13 [hp_X]/mLValerian — 6 [hp_X]/mLAllylthiourea — 6 [hp_X]/mLPassiflora incarnata flower — 5 [hp_X]/mL
Dosage form: Liquid
Route: Auricular (Otic)
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 19, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 17312-175_46065bc3-19db-9699-e063-6394a90a386fSPL ID 46065bc3-19db-9699-e063-6394a90a386fSPL set ID 92ef0dd1-84f9-086c-e053-2a95a90ac647UNII O80TY208ZW, 1MBW07J51Q, XK4IUX8MNB, C88X29Y479, G0R4UBI2ZZ, O414PZ4LPZ, ETJ7Z6XBU4, JWF5YAW3QW, 706IDJ14B7, K8F3G29S6ZUPC 0858961001754

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

N417312017515 followed by a unit qualifier and the quantity

Package 17312-0175-15. 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 provide temporary relief from symptoms such as: • Ringing, buzzing, roaring • Nerve and noise sensitivity • Pounding • Discomfort • Wax buildup • Sleeplessness; 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 17312-175

What is NDC 17312-175?: 17312-175 is the product NDC for Ring Relief PM Nighttime Formula, Arnica montana 6 [hp_X]/mL + 9 more ingredients liquid, 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 PM Nighttime Formula (Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea).
What is the active ingredient?: Arnica montana, Calcium sulfide, Hypericum perforatum, Lycopodium clavatum spore, Matricaria chamomilla, Salicylic acid, Silicon dioxide, Valerian, Allylthiourea, Passiflora incarnata flower.
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 PM Nighttime Formula?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.