Home NDC 10733-412 lumicain
Product NDC 10733-412
11-digit product format 107330412
Labeler code 10733
Product ID 10733-412_b725dd26-c793-51a4-e053-2a95a90a573d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Aluminium Chloride Hexahydrate
Dosage form SOLUTION
Route TOPICAL
Labeler Medical Products Laboratories, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2010-09-29
Substance ALUMINUM CHLORIDE
Active strength 250 mg/g
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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 10733-412-60 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 10733-412-60 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 10733-412-60 110d247fa046…a55b01930146…
Additional Listing Data#
Finished product Yes
Brand name base lumicain
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM CHLORIDE 250 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3CYT62D3GA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 244613 Internal RxNorm lookup 486109 Internal RxNorm 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 10733-412-60 lumicain 67 g in 1 BOTTLE SOLUTION 67 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10733-412 LUMICAIN (ALUMINIUM CHLORIDE HEXAHYDRATE) SOLUTION [MEDICAL PRODUCTS LABORATORIES, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20201224_9fdcce3e-e4d4-41ae-8609-37987c12414e.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.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join lumicain ALUMINIUM CHLORIDE HEXAHYDRATE Medical Products Laboratories, Inc. 9fdcce3e-e4d4-41ae-8609-37987c12414e 2020-12-23 Warnings Exact identifier ndc (product): 10733-412
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 10733-412-60 10733041260 67 g in 1 BOTTLE (10733-412-60) 67 g 2020-09-29 0000-00-00 No No Current