Home NDC 69903-002 Dr. Numb
Product NDC 69903-002
11-digit product format 699030002
Labeler code 69903
Product ID 69903-002_50b50aba-23c0-623d-e063-6394a90ab2eb
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine and Benzethonium Chloride Cream
Dosage form CREAM
Route TOPICAL
Labeler Shinpharma Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-09-12
Substance LIDOCAINE; BENZETHONIUM CHLORIDE
Active strength 4; .25 mg/50g; mg/50g
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 · 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 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 69903-002 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69903-002 69903-002-50 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 Dr. Numb
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 4 mg/50g BENZETHONIUM CHLORIDE .25 mg/50g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup PH41D05744 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69903-002-50 Dr. Numb 1 in 1 CARTRIDGE CREAM 1 6 69903-002-50 Dr. Numb 50 g in 1 TUBE CREAM 50 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69903-002 DR. NUMB (LIDOCAINE AND BENZETHONIUM CHLORIDE CREAM) CREAM [SHINPHARMA INC] 5 Current NDC, Legacy NDC, 2 package rows 20240405_d8cdccdb-775b-4970-a6ea-50b62df221d6.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 111 of 152 · 3,029 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69903-002-50 69903000250 1 TUBE in 1 CARTRIDGE (69903-002-50) / 50 g in 1 TUBE 1 tube 2017-09-12 0000-00-00 No No Current