Home NDC 79804-282 Pain Relief Roll On
Product NDC 79804-282
11-digit product format 798040282
Labeler code 79804
Product ID 79804-282_485aeef9-80db-6a7b-e063-6394a90a1477
Type HUMAN OTC DRUG
Nonproprietary name Topical Analgesic
Dosage form LIQUID
Route TOPICAL
Labeler Eagle Labs Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-11-07
Substance MENTHOL; CAMPHOR (SYNTHETIC); CAPSAICIN
Active strength .06; .05; .00025 g/g; g/g; g/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 79804-282 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 79804-282 79804-282-03 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 Roll On
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL .06 g/g CAMPHOR (SYNTHETIC) .05 g/g CAPSAICIN .00025 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup 5TJD82A1ET Internal UNII lookup S07O44R1ZM Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2610122 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79804-282-03 Pain Relief Roll On 87 g in 1 PACKAGE LIQUID 87 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79804-282 PAIN RELIEF ROLL ON (TOPICAL ANALGESIC) LIQUID [EAGLE LABS INC] 3 Current NDC, Legacy NDC, 1 package rows 20240418_2380a400-062a-4a8d-a594-a2e097219044.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 23 of 153 · 3,057 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kevo-Prophen JUNIPER TAR Faeve, LLC 4fe773a8-77cd-831e-e063-6294a90ae2ca 2026-04-20 Warnings Exact identifier application number: M017 BeeVenom METHYL SALICYLATE Menper Distributors, Inc. 4fe7a986-336d-ad4e-e063-6294a90a0b8a 2026-04-20 Warnings Exact identifier application number: M017 Benzodent BENZOCAINE Focus Consumer Healthcare, LLC 5fdcb871-d387-6352-e053-2991aa0a09da 2026-04-20 Warnings Exact identifier application number: M017 Tecnu Calagel DIPHENHYDRAMINE HYDROCHLORIDE Tec Laboratories Inc. 8bc9cbfe-1dd4-18ed-e053-2a95a90a7966 2026-04-20 Warnings Exact identifier application number: M017 Aemerry Numbing Cream MENTHOL 5% Da Capo Prima LLC 4fefddaf-19c8-86b4-e063-6294a90abffc 2026-04-20 Warnings Exact identifier application number: M017 Sting Relief Swab BENZOCAINE 4 Visions LLC 4fc7a356-2f1d-85af-e063-6394a90aec6b 2026-04-18 Warnings Exact identifier application number: M017 Equate Lidocaine and Menthol Paraben Free LIDOCAINE 4% PLUS MENTHOL 1% Walmart Stores Inc 4fa917de-bc46-0b8d-e063-6294a90a218a 2026-04-17 Warnings Exact identifier application number: M017 LidoPro LIDOCAINE AND MENTHOL Advanced Rx of Tennessee, LLC 4faa515f-6040-d948-e063-6294a90a187f 2026-04-17 Warnings Exact identifier application number: M017 Coleman Bite and Sting Relief EXTERNAL ANESTHETIC AND FIRST AID ANTISEPTIC Wisconsin Pharmacal Company 4fadf1f1-478a-5104-e063-6294a90a10cb 2026-04-17 Warnings Exact identifier application number: M017 Ice Gel ICE COLD ANALGESIC MENTHOL Universal Distribution Center LLC 4f921ced-7722-cba5-e063-6294a90a650b 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Capsaicin Hot Patch CAPSAICIN Walgreen Co. 41e959d8-f6ac-f5b4-e063-6294a90abd96 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Cold Therapy Pain Relieving Patch MENTHOL Walgreen Co. 41e7574a-348f-8eb8-e063-6294a90a6e90 2026-04-16 Warnings Exact identifier application number: M017 Coleman Sting and Bite Relief EXTERNAL ANALGESIC AND FIRST AID ANTISEPTIC Wisconsin Pharmacal Company 4f94ab35-3099-716c-e063-6294a90a8bea 2026-04-16 Warnings Exact identifier application number: M017 Kroger Witch Hazel WITCH HAZEL Kroger Co. 461407d0-fbf6-47e9-e063-6394a90a9a83 2026-04-16 Warnings Exact identifier application number: M017 Stopain Extra Strength Gel MENTHOL Troy Manufacturing, Inc. 86fe4e8c-5279-445a-a19a-e694eac785fd 2026-04-16 Warnings Exact identifier application number: M017 Stopain Clinical MENTHOL, UNSPECIFIED FORM Troy Manufacturing, Inc. 4503208f-2808-4727-8066-c431230bd70b 2026-04-16 Warnings Exact identifier application number: M017 EXTRA STRENGTH STOPAIN COLD PAIN RELIEVING ROLL ON MENTHOL TROY MANUFACTURING, INC 895896dc-0762-40a7-8313-cca10ce68984 2026-04-16 Warnings Exact identifier application number: M017 HealthWise Medicated Cold Hot 5% MENTHOL Veridian Healthcare 4f9b1b2d-1acc-e0a7-e063-6394a90aadbc 2026-04-16 Warnings Exact identifier application number: M017 Lidoease 2% LIDOCAINE HCL 2% PureTek Corporation 3ba0c0ff-0f7a-7a29-e063-6294a90a547a 2026-04-16 Warnings Exact identifier application number: M017 Walgreens Lidocaine Pain Relieving Patch Assorted LIDOCAINE Walgreen Co. 41e98f15-669f-4543-e063-6294a90a1ef7 2026-04-15 Warnings Exact identifier application number: M017
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 79804-282-03 79804028203 87 g in 1 PACKAGE (79804-282-03) 87 g 2022-11-07 0000-00-00 No No Current