United States · FDA National Drug Code directory

Ring Relief

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 17312-001_46065bc3-19da-9699-e063-6394a90a386f
Product NDC: 17312-001
Form: LIQUID
Composition / generic term: Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea
Labeler: TRP Company
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20060601
Source listing expiry: 20261231

Source-listed ingredients

ARNICA MONTANA — 6 [hp_X]/mL
CALCIUM SULFIDE — 13 [hp_X]/mL
HYPERICUM PERFORATUM — 6 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE — 12 [hp_X]/mL
MERCURIUS SOLUBILIS — 13 [hp_X]/mL
SALICYLIC ACID — 6 [hp_X]/mL
SILICON DIOXIDE — 13 [hp_X]/mL
ALLYLTHIOUREA — 6 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE, DROPPER in 1 PACKAGE (17312-001-15) / 10 mL in 1 BOTTLE, DROPPER · 17312-001-15

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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