Home NDC 82988-102-04 Ice Blue Pain Alleviating Rub
Product NDC 82988-102
Requested package NDC 82988-102-04
11-digit product format 829880102
Labeler code 82988
Product ID 82988-102_c8b1a1f6-4e27-4e37-b0cd-6171939fd038
Type HUMAN OTC DRUG
Nonproprietary name MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)
Dosage form SPRAY
Route TOPICAL
Labeler Lemisol Corporation
Application part348
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2022-08-31
Marketing end 0000-00-00
Substance CAMPHOR (NATURAL); MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE
Active strength 0 g/g; g/g; g/g
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 15 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82988-102 ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) GEL ICE BLUE PAIN ALLEVIATING RUB (MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, CAMPHOR (NATURAL)) SPRAY [LEMISOL CORPORATION] 1 Legacy NDC 20221221_0238f4aa-6f40-489a-9a09-a6ba2d8080b5.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 82988-102-04 82988010204 118.2 g in 1 BOTTLE, SPRAY (82988-102-04) 118.2 g 2022-08-31 0000-00-00 No No Current