Home NDC 11673-910 UpandUp
Product NDC 11673-910
11-digit product format 116730910
Labeler code 11673
Product ID 11673-910_3a0c4aac-ed7d-1c51-e063-6294a90a5a99
Type HUMAN OTC DRUG
Nonproprietary name Clotrimazole
Dosage form CREAM
Route TOPICAL
Labeler Target Corporation
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 1993-08-31
Substance CLOTRIMAZOLE
Active strength 10 mg/g
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS]
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 · 3 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 product product 11673-910 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 11673-910 11673-910-12 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 11673-910 11673-910-16 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
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 UpandUp
Brand name suffix Clotrimazole
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CLOTRIMAZOLE 10 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G07GZ97H65 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 309367 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 11673-910-02 UpandUpClotrimazole 1 in 1 CARTON CREAM 1 6 11673-910-02 UpandUpClotrimazole 28.4 g in 1 TUBE CREAM 28.4 6 11673-910-12 UpandUpClotrimazole 1 in 1 CARTON CREAM 1 6 11673-910-12 UpandUpClotrimazole 30 g in 1 TUBE CREAM 30 6 11673-910-16 UpandUpClotrimazole 1 in 1 CARTON CREAM 1 6 11673-910-16 UpandUpClotrimazole 40 g in 1 TUBE CREAM 40 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-910 UPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION] 5 Current NDC, Legacy NDC, 6 package rows 20241115_cb2b7d38-9988-493b-9843-56c2f59eed2f.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 11673-910-02 11673091002 1 TUBE in 1 CARTON (11673-910-02) / 28.4 g in 1 TUBE 1 tube 2020-09-30 0000-00-00 No No Current 11673-910-12 11673091012 1 TUBE in 1 CARTON (11673-910-12) / 30 g in 1 TUBE 1 tube 2013-01-14 0000-00-00 No No Current 11673-910-16 11673091016 1 TUBE in 1 CARTON (11673-910-16) / 40 g in 1 TUBE 1 tube 2013-01-14 0000-00-00 No No Current