Home NDC 77496-101-11 ProloGel Pain Relief
Product NDC 77496-101
Requested package NDC 77496-101-11
11-digit product format 774960101
Labeler code 77496
Product ID 77496-101_ff163568-addd-41b7-b99d-22fa5dff2f7b
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC) and SODIUM BICARBONATE
Dosage form LOTION
Route TOPICAL
Labeler Nova Neura, LLC
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2020-12-01
Marketing end 0000-00-00
Substance CAMPHOR (SYNTHETIC); SODIUM BICARBONATE
Active strength 0 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2022-12-31
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.
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 77496-101-11 ProloGel Pain Relief 148 mL in 1 BOTTLE, PUMP LOTION 148 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 77496-101 PROLOGEL PAIN RELIEF (CAMPHOR (SYNTHETIC) AND SODIUM BICARBONATE) LOTION [NOVA NEURA, LLC] 2 Legacy NDC, 1 package rows 20210905_a1741cbb-37a6-485d-9d62-5e096ddffa0e.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 77496-101-11 77496010111 148 mL in 1 BOTTLE, PUMP (77496-101-11) 148 ml 2020-12-01 0000-00-00 No No Current