Home NDC 69993-350 Blue-Emu Lidocaine Pain Relief Cream
Product NDC 69993-350
11-digit product format 699930350
Labeler code 69993
Product ID 69993-350_26d51c7f-f593-4761-ae9d-6d8b791fb18c
Type HUMAN OTC DRUG
Nonproprietary name lidocaine cream 4%
Dosage form CREAM
Route TOPICAL
Labeler Kingsway Pharmaceuticals dba NFI, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-03-01
Substance LIDOCAINE HYDROCHLORIDE
Active strength 40 mg/1
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 · 2 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 2021-12-27 23:28 UTC · source 2021-12-27 excluded product product 69993-350 I Inactivated by FDA excluded / ndc_excluded.zip 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 69993-350 69993-350-03 I Inactivated by FDA excluded / ndc_excluded.zip 8dfbde2a14a4…c9ff85d89658…
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 Blue-Emu Lidocaine Pain Relief Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE HYDROCHLORIDE 40 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1421893 Internal RxNorm 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 69993-350-03 Blue-Emu Lidocaine Pain Relief Cream 77 in 1 TUBE CREAM 77 12 69993-350-03 Blue-Emu Lidocaine Pain Relief Cream 1 in 1 CARTON CREAM 1 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69993-350 BLUE-EMU LIDOCAINE PAIN RELIEF CREAM (LIDOCAINE CREAM 4%) CREAM [KINGSWAY PHARMACEUTICALS DBA NFI, LLC] 11 Current NDC, Legacy NDC, 2 package rows 20250209_592811f2-e21c-6a58-e053-2991aa0a69a9.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.
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 69993-350-03 69993035003 1 TUBE in 1 CARTON (69993-350-03) / 77 CREAM in 1 TUBE 1 tube 2017-03-01 0000-00-00 No No Current