Home NDC 79804-282-03 Pain Relief Roll On
Product NDC 79804-282
Requested package NDC 79804-282-03
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 · 1 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 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 111 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HealthWise Medicated Original Body Powder 10 oz MENTHOL Veridian Healthcare 296b623a-14cd-0bca-e063-6394a90ac5ff 2024-12-16 Warnings Exact identifier application number: M017 HealthWise Medicated Extra Body Powder 10 oz MENTHOL Veridian Healthcare 296c9a9c-e3db-59fe-e063-6294a90a0b62 2024-12-16 Warnings Exact identifier application number: M017 Rite Aid Hot and Cold Roll On MENTHOL 16% Rite Aid fc4b2635-280b-267f-e053-6294a90a5e22 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Pain Relieving BENZOCAINE 20%, MENTHOL 0.5% Rite Aid e2c09e85-be0a-4e6d-e053-2995a90ad756 2024-12-15 Warnings Exact identifier application number: M017 Rugby Lidocaine LIDOCAINE 4% Rugby Laboratories d94292f7-10fc-48bf-e053-2995a90a8472 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Cortisone HYDROCORTISONE 1% Rite Aid e27353b9-23b6-3801-e053-2a95a90a6045 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Cooling Pain Relief MENTHOL 10.5% Rite Aid e2225259-70ec-52de-e053-2a95a90a73f8 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Rectal Care LIDOCAINE 5% Rite Aid e283e462-96e8-04cf-e053-2a95a90a1d00 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Anti-Itch DIPHENHYDRAMINE HCL 2% Rite Aid e33898d8-1b8b-5c0b-e053-2995a90add08 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Cala Itch Relief PRAMOXINE HCL 1%, ZINC ACETATE 0.1% Rite Aid e29a9d59-4c7c-81aa-e053-2995a90a7056 2024-12-15 Warnings Exact identifier application number: M017 CVS Roll-On CAPSAISIN 0.1% CVS e8812c49-335e-61ea-e053-2995a90a17aa 2024-12-15 Warnings Exact identifier application number: M017 Good Sense Burn Relief Aloe LIDOCAINE HCL Geiss, Destin & Dunn, Inc b5a7f629-a88d-b49d-e053-2995a90a49fa 2024-12-15 Warnings Exact identifier application number: M017 QC Burn Relief Aloe LIDOCAINE HCL Chain Drug Marketing Association Inc b5e76f0c-0bfe-b13e-e053-2995a90a0861 2024-12-15 Warnings Exact identifier application number: M017 Meijer Burn Relief LIDOCAINE 0.5% Meijer bec60c93-5abd-ee04-e053-2a95a90acb61 2024-12-15 Warnings Exact identifier application number: M017 QC Cool and Heat Roll-On MENTHOL 16% Chain Drug Marketing Association Inc d35e9dfa-8a28-fdb3-e053-2995a90abc52 2024-12-15 Warnings Exact identifier application number: M017 Meijer Cold and Hot Pain Relieving MENTHOL 16% Meijer bec62df3-06c9-a115-e053-2995a90a4267 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief MENTHOL 16% Tommie Copper, Inc. b4dfa5fa-2d61-db1e-e053-2a95a90a7ac8 2024-12-15 Warnings Exact identifier application number: M017 Pain Relief Liquid Roller CAMPHOR 3.5%, MENTHOL 3.5% Tommie Copper, Inc. c9f0447e-de43-16a5-e053-2995a90a05c1 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief Maximum Strength TROLAMINE SALICYLATE 10% Tommie Copper, Inc. b622c14f-9bf3-0bbd-e053-2a95a90a2adc 2024-12-15 Warnings Exact identifier application number: M017 Copperlife Pain Relief TROLAMINE SALICYLATE 10% Tommie Copper, Inc. c94d00f9-42ce-1d43-e053-2a95a90a058d 2024-12-15 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