Home NDC 10733-415-40 Salinocaine
Product NDC 10733-415
Requested package NDC 10733-415-40
11-digit product format 107330415
Labeler code 10733
Product ID 10733-415_1f19cc2c-57ab-4ad4-e063-6294a90a7613
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name salicylic acid and benzocaine
Dosage form OINTMENT
Route TOPICAL
Labeler Medical Products Laboratories, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1938-06-01
Substance BENZOCAINE; SALICYLIC ACID
Active strength 20; 550 mg/g; mg/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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 2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 10733-415 10733-415-40 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 10733-415 10733-415-40 E Excluded after deficient or non-compliant submission was not corrected excluded / ndc_excluded.zip 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base Salinocaine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 550 mg/g BENZOCAINE 20 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup U3RSY48JW5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1603377 Internal RxNorm lookup 1603382 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 10733-415-40 Salinocaine 40 g in 1 JAR OINTMENT 40 9
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10733-415 SALINOCAINE (SALICYLIC ACID AND BENZOCAINE) OINTMENT [MEDICAL PRODUCTS LABORATORIES, INC.] 9 Current NDC, Legacy NDC, 1 package rows 20240809_49d9f83d-3055-f80e-e58a-b6fca192ac8d.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 1 of 1 · 1 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 10733-415-40 10733041540 40 g in 1 JAR (10733-415-40) 40 g 1938-06-01 0000-00-00 No No Current