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 127 of 153 · 3,057 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 79804-282-03 79804028203 87 g in 1 PACKAGE (79804-282-03) 87 g 2022-11-07 0000-00-00 No No Current