Home NDC 72854-682 KY
Product NDC 72854-682
11-digit product format 728540682
Labeler code 72854
Product ID 72854-682_51e0d87a-5f9f-a7ef-e063-6394a90a90b4
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine
Dosage form SPRAY, METERED
Route TOPICAL
Labeler Reckitt Benckiser LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-08-01
Substance LIDOCAINE
Active strength 96 mg/mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 · 3 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 72854-682 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 72854-682 72854-682-10 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 72854-682 72854-682-01 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 KY
Brand name suffix Duration for Him
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 96 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII 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 72854-682-01 KYDuration for Him 1 in 1 CARTON SPRAY, METERED 1 5 72854-682-01 KYDuration for Him 5 mL in 1 BOTTLE, SPRAY SPRAY, METERED 5 5 72854-682-10 KYDuration for Him 10.8 mL in 1 BOTTLE, SPRAY SPRAY, METERED 10.8 5 72854-682-10 KYDuration for Him 1 in 1 CARTON SPRAY, METERED 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72854-682 KY DURATION FOR HIM (LIDOCAINE) SPRAY, METERED [RB HEALTH (US) LLC] 4 Current NDC, Legacy NDC, 4 package rows 20250215_83cc86bd-3303-4956-a198-fae85b6e34e1.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 18 of 153 · 3,057 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 72854-682-01 72854068201 1 BOTTLE, SPRAY in 1 CARTON (72854-682-01) / 5 mL in 1 BOTTLE, SPRAY 2020-08-01 0000-00-00 No No Current 72854-682-10 72854068210 1 BOTTLE, SPRAY in 1 CARTON (72854-682-10) / 10.8 mL in 1 BOTTLE, SPRAY 2022-02-20 0000-00-00 No No Current