Home NDC 11523-0012 Lotrimin Daily Sweat and Odor Control
Product NDC 11523-0012
11-digit product format 115230012
Labeler code 11523
Product ID 11523-0012_488511a8-cba1-6c74-e063-6294a90af1a3
Type HUMAN OTC DRUG
Nonproprietary name topical starch
Dosage form POWDER
Route TOPICAL
Labeler Bayer HealthCare LLC.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-02-17
Substance STARCH, CORN
Active strength 837 mg/g
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 · 4 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 11523-0012-1 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 11523-0012-1 f5e01cc5f278…a2eaf40c39c3…
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 Lotrimin Daily Sweat and Odor Control
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength STARCH, CORN 837 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O8232NY3SJ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1294098 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 11523-0012-1 Lotrimin Daily Sweat and Odor Control 177 g in 1 BOTTLE POWDER 177 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11523-0012 LOTRIMIN DAILY SWEAT AND ODOR CONTROL (TOPICAL STARCH) POWDER [BAYER HEALTHCARE LLC.] 5 Current NDC, Legacy NDC, 1 package rows 20241208_9ec5c80d-b550-496f-e053-2a95a90a5489.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 8 of 49 · 973 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 11523-0012-1 11523001201 177 g in 1 BOTTLE (11523-0012-1) 177 g 2020-02-17 0000-00-00 No No Current