Home NDC 69968-0487 Bengay Ultra Strength
Product NDC 69968-0487
11-digit product format 699680487
Labeler code 69968
Product ID 69968-0487_21ff7385-a28f-c8fc-e063-6394a90abdfe
Type HUMAN OTC DRUG
Nonproprietary name Menthol, Unspecified Form
Dosage form PATCH
Route TOPICAL
Labeler Kenvue Brands LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-03
Substance MENTHOL, UNSPECIFIED FORM
Active strength 50 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
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 · 12 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…
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 Bengay Ultra Strength
Brand name suffix Large Size
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL, UNSPECIFIED FORM 50 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 420222 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69968-0487-1 Bengay Ultra StrengthLarge Size 1 in 1 POUCH PATCH 1 7 69968-0487-1 Bengay Ultra StrengthLarge Size 1 in 1 CARTON PATCH 1 7 69968-0487-4 Bengay Ultra StrengthLarge Size 1 in 1 POUCH PATCH 1 7 69968-0487-4 Bengay Ultra StrengthLarge Size 4 in 1 CARTON PATCH 4 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69968-0487 BENGAY ULTRA STRENGTH LARGE SIZE (MENTHOL, UNSPECIFIED FORM) PATCH [KENVUE BRANDS LLC] 7 Current NDC, Legacy NDC, 4 package rows 20241108_f57ccc33-400b-4401-a348-c54d1eb9f5d0.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 112 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 69968-0487-1 69968048701 1 POUCH in 1 CARTON (69968-0487-1) > 1 PATCH in 1 POUCH 1 pouch 2019-04-03 0000-00-00 No No Current 69968-0487-4 69968048704 4 POUCH in 1 CARTON (69968-0487-4) / 1 PATCH in 1 POUCH 4 pouch 2019-09-01 0000-00-00 No No Current