FDA.reportPublic FDA data

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 dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct11673-910IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage11673-91011673-910-12IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage11673-91011673-910-16IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…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
IngredientStrength
CLOTRIMAZOLE10 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
G07GZ97H65Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
309367Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
cb2b7d38-9988-493b-9843-56c2f59eed2fAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b64d2752-34ef-378a-1f4f-8bff32b0d1aeProduct name420250626
cb7783e0-feaa-7e56-fb3b-d43b6efa77c9Product name220250121
f31c883b-7ebf-1c60-f3b6-4ba41e8ff7a6Product name220151106
f5395dd2-4395-d8c6-3477-8c2d4a2f951cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
11673-910-122020-10-15Up&Up Clotrimazole 1%
11673-910-162020-10-15Up&Up Clotrimazole 1%
11673-910-122020-01-31Up&Up Clotrimazole 1%
11673-910-162020-01-31Up&Up Clotrimazole 1%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-910-02UpandUpClotrimazole1 in 1 CARTONCREAM16
11673-910-02UpandUpClotrimazole28.4 g in 1 TUBECREAM28.46
11673-910-12UpandUpClotrimazole1 in 1 CARTONCREAM16
11673-910-12UpandUpClotrimazole30 g in 1 TUBECREAM306
11673-910-16UpandUpClotrimazole1 in 1 CARTONCREAM16
11673-910-16UpandUpClotrimazole40 g in 1 TUBECREAM406

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
11673-910-12GM - Gram11673-91099a9e499-aa74-46c5-988e-8f12dbf3476f12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ClotrimazoleACTIVE INGREDIENTG07GZ97H65UPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
ClotrimazoleACTIVE MOIETYG07GZ97H65UPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
benzyl alcoholINACTIVE INGREDIENTLKG8494WBHUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
cetostearyl alcoholINACTIVE INGREDIENT2DMT128M1SUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
cetyl esters waxINACTIVE INGREDIENTD072FFP9GUUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
octyldodecanolINACTIVE INGREDIENT461N1O614YUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
polysorbate 60INACTIVE INGREDIENTCAL22UVI4MUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
sorbitan monostearateINACTIVE INGREDIENTNVZ4I0H58XUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3
waterINACTIVE INGREDIENT059QF0KO0RUPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-910UPANDUP CLOTRIMAZOLE (CLOTRIMAZOLE) CREAM [TARGET CORPORATION]5Current NDC, Legacy NDC, 6 package rows20241115_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 34 of 49 · 973 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ClotrimazoleCLOTRIMAZOLEAvPAK3ca3b475-7b69-442a-e063-6294a90a7b3f2025-08-18WarningsExact identifier
application number: M005
Formula 3TOLNAFTATEThe Tetra Corporation0895274b-a09d-4264-a43f-852e44eb31632025-08-18WarningsExact identifier
application number: M005
Formula 7 - The SolutionTOLNAFTATEThe Tetra Corporation18619649-7f79-4b6e-8b7c-69d70365d5572025-08-18WarningsExact identifier
application number: M005
GlyCylicSALICYLIC ACIDThe Tetra Corporation501d3ba9-ba42-4c1c-983b-492adaee039d2025-08-18WarningsExact identifier
application number: M005
SupreH Ringworm Treatment BalmSUPREH RINGWORM TREATMENT BALMShenzhen Xinxin Yunhai Technology Co., Ltd.3c77222b-d92e-84b0-e063-6294a90aadd72025-08-16WarningsExact identifier
application number: M005
OetMoe Antifungal SolutionOETMOE ANTIFUNGAL SOLUTIONShenzhen Earth Surface Trading Co., Ltd.3c26d917-4186-6f02-e063-6394a90a99f62025-08-12WarningsExact identifier
application number: M005
Cureforte Anti Fungal Foot CareANTI FUNGAL FOOT CARE DROPSSTEEL CITY HEALTH PRIVATE LIMITED39f762a6-9d0c-8ded-e063-6394a90a36592025-08-11WarningsExact identifier
application number: M005
Derman Antifungal Powder TolnaftateTOLNAFTATETaisho Pharmaceutical California Inc.3a854765-740c-4719-8abf-4b3f932cdee02025-08-07WarningsExact identifier
application number: M005
Derman antifungal creamTOLNAFTATETaisho Pharmaceutical California Inc.15d9b3c9-01af-4083-a1bc-014505d8798d2025-08-07WarningsExact identifier
application number: M005
Maximum Strength Antifungal LiquidTOLNAFTATEHudson Health LLC24b22794-f9f8-6f32-e063-6394a90aec982025-08-07WarningsExact identifier
application number: M005
Toe Area TreatmentTOLNAFTATECVS17681cc8-fbb1-a0cf-e063-6294a90add182025-08-07WarningsExact identifier
application number: M005
Antifungal LiquidTOLNAFTATEFamily Dollar Services, Inc178e7b3f-949f-3f51-e063-6294a90a93952025-08-07WarningsExact identifier
application number: M005
Antifungal LiquidTOLNAFTATELEADER/Cardinal Health 110, Inc.17695563-3765-74cb-e063-6294a90a61202025-08-07WarningsExact identifier
application number: M005
Antifungal LiquidTOLNAFTATETarget Corporation1dff278f-47bc-459a-e063-6394a90a26462025-08-07WarningsExact identifier
application number: M005
Antifungal LiquidTOLNAFTATETopCo Associates19c268a1-7b2e-63c9-e063-6394a90acddc2025-08-07WarningsExact identifier
application number: M005
Antifungal Liquid Maximum StrengthTOLNAFTATEWalgreens Company137eabb7-cb4f-1631-e063-6294a90ab8472025-08-07WarningsExact identifier
application number: M005
WCTNGO Fungal Nail Treatment SwabsTOLNAFTATE,UNDECYLENIC ACIDShenzhen Boyimei Technology Co., Ltd.3bad0d73-b33d-b962-e063-6294a90a7ba72025-08-06WarningsExact identifier
application number: M005
ONIADBA Nail Fungus Treatment PenTOLNAFTATE,UNDECYLENIC ACIDShenzhen Boyimei Technology Co., Ltd.3bad19f1-d5b3-c5de-e063-6294a90a0c032025-08-06WarningsExact identifier
application number: M005
Antifungal LiquidTOLNAFTATEPremier Brands of America Inc2644ba07-aaee-6402-e063-6394a90a28272025-08-06WarningsExact identifier
application number: M005
Anti- Fungal Miconazole NitrateMICONAZOLE NITRATEPremier Brands of America Inc.f186bdc1-db6c-0fab-e053-2995a90a7c582025-08-06WarningsExact identifier
application number: M005

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
309367clotrimazole 1 % Topical CreamPSNcb2b7d38-9988-493b-9843-56c2f59eed2f6
309367clotrimazole 10 MG/ML Topical CreamSCDcb2b7d38-9988-493b-9843-56c2f59eed2f6
309367clotrimazole 1 % Topical CreamSYcb2b7d38-9988-493b-9843-56c2f59eed2f6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-910-02116730910021 TUBE in 1 CARTON (11673-910-02) / 28.4 g in 1 TUBE1 tube2020-09-300000-00-00NoNoCurrent
11673-910-12116730910121 TUBE in 1 CARTON (11673-910-12) / 30 g in 1 TUBE1 tube2013-01-140000-00-00NoNoCurrent
11673-910-16116730910161 TUBE in 1 CARTON (11673-910-16) / 40 g in 1 TUBE1 tube2013-01-140000-00-00NoNoCurrent