Home FDA labels 46065bc3-19db-9699-e063-6394a90a386f Ring Relief PM Nighttime Formula openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Ring Relief PM Nighttime Formula
Generic name ARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, THIOSINAMINUM, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREA
Manufacturer TRP Company
Product type HUMAN OTC DRUG
SPL set ID 92ef0dd1-84f9-086c-e053-2a95a90ac647
SPL ID 46065bc3-19db-9699-e063-6394a90a386f
Version 5
Effective date 2025-12-15
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:31 Harmonized routes table Harmonized routes AURICULAR (OTIC)
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 18 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Ring Relief PM Nighttime Formula openfda.brand_name generic name ARNICA MONTANA, CALCIUM SULFIDE, HYPERICUM PERFORATUM, LYCOPODIUM CLAVATUM SPORE, THIOSINAMINUM, MERCURIUS SOLUBILIS, SALICYLIC ACID, SILICON DIOXIDE, ALLYLTHIOUREA openfda.generic_name manufacturer name TRP Company openfda.manufacturer_name ndc package 17312-175-15 openfda.package_ndc ndc product 17312-175 openfda.product_ndc ndc11 package 17312017515 derived:openfda.package_ndc spl id 46065bc3-19db-9699-e063-6394a90a386f id spl set id 92ef0dd1-84f9-086c-e053-2a95a90ac647 set_id unii XK4IUX8MNB openfda.unii unii O80TY208ZW openfda.unii unii O414PZ4LPZ openfda.unii unii ETJ7Z6XBU4 openfda.unii unii JWF5YAW3QW openfda.unii unii 706IDJ14B7 openfda.unii unii G0R4UBI2ZZ openfda.unii unii K8F3G29S6Z openfda.unii unii C88X29Y479 openfda.unii unii 1MBW07J51Q openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings: A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. For External Use Only. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur. Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.