Home NDC 64092-403-04 nasal decongestant
Product NDC 64092-403
Requested package NDC 64092-403-04
11-digit product format 640920403
Labeler code 64092
Product ID 64092-403_39573c12-c132-10cb-e054-00144ff88e88
Type HUMAN OTC DRUG
Nonproprietary name Menthol, camphor,eucalyptus oil
Dosage form GEL
Route TOPICAL
Labeler Great Lakes Wholesale, Marketing, and Sales, INC
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2016-06-30
Marketing end 0000-00-00
Substance CAMPHOR (SYNTHETIC); EUCALYPTUS OIL; MENTHOL
Active strength 5 1/110g; 1/110g; 1/110g
NDC exclude flag No
Listing certified through 2020-12-31
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64092-403-04 nasal decongestant 110 g in 1 JAR GEL 110 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64092-403 NASAL DECONGESTANT (MENTHOL, CAMPHOR,EUCALYPTUS OIL) GEL [GREAT LAKES WHOLESALE, MARKETING, AND SALES, INC] 1 Legacy NDC, 1 package rows 20160806_39573c12-c131-10cb-e054-00144ff88e88.zip
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 64092-403-04 64092040304 110 g in 1 JAR (64092-403-04) 110 g 2016-06-30 0000-00-00 No No Current