FDA.reportPublic FDA data

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Product NDC
63736-532
11-digit product format
637360532
Labeler code
63736
Product ID
63736-532_782d859a-fbb0-4049-a6f4-7f92596bb865
Type
HUMAN OTC DRUG
Nonproprietary name
Miconazole Nitrate
Dosage form
AEROSOL, POWDER
Route
TOPICAL
Labeler
Insight Pharmaceuticals LLC
Application
part333C
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2009-07-16
Marketing end
0000-00-00
Substance
MICONAZOLE NITRATE
Active strength
3 g/128g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct63736-532DDiscontinued by firm2026-10-21
excluded packagepackage63736-53263736-532-05DDiscontinued by firm2026-10-21

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 dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage63736-532-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage63736-532-05f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2023-03-02Ting Spray Powder
2023-01-30Ting Spray Powder
2020-04-13Ting Spray Powder
2020-01-31Ting Spray Powder

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Miconazole NitrateACTIVE INGREDIENTVW4H1CYW1KTING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
MiconazoleACTIVE MOIETY7NNO0D7S5MTING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
Aloe vera leafINACTIVE INGREDIENTZY81Z83H0XTING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
IsobutaneINACTIVE INGREDIENTBXR49TP611TING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
isopropyl myristateINACTIVE INGREDIENT0RE8K4LNJSTING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
PropaneINACTIVE INGREDIENTT75W9911L6TING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
propylene carbonateINACTIVE INGREDIENT8D08K3S51ETING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2
sorbitan monooleateINACTIVE INGREDIENT06XEA2VD56TING SPRAY POWDER (MICONAZOLE NITRATE) AEROSOL, POWDER [INSIGHT PHARMACEUTICALS]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63736-532-0563736053205128 g in 1 CAN (63736-532-05) 128 g2009-07-160000-00-00NoNoCurrent