Home NDC 72562-167 Pain Relief Liquid Roller
Product NDC 72562-167
11-digit product format 725620167
Labeler code 72562
Product ID 72562-167_29591578-c164-5ed4-e063-6394a90a7df3
Type HUMAN OTC DRUG
Nonproprietary name Camphor 3.5%, Menthol 3.5%
Dosage form LIQUID
Route TOPICAL
Labeler Tommie Copper, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-08-19
Substance MENTHOL; CAMPHOR (SYNTHETIC)
Active strength 3.5; 3.5 g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Pain Relief Liquid Roller
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 3.5 g/100g CAMPHOR (SYNTHETIC) 3.5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 5TJD82A1ET Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2467741 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72562-167-25 Pain Relief Liquid Roller 70 g in 1 BOTTLE, PLASTIC LIQUID 70 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72562-167 PAIN RELIEF LIQUID ROLLER (CAMPHOR 3.5%, MENTHOL 3.5%) LIQUID [TOMMIE COPPER, INC.] 3 Current NDC, Legacy NDC, 1 package rows 20241217_c9f0447e-de43-16a5-e053-2995a90a05c1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 8 of 156 · 3,115 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72562-167-25 72562016725 70 g in 1 BOTTLE, PLASTIC (72562-167-25) 70 g 2021-08-19 0000-00-00 No No Current