FDA.reportPublic FDA data

Aplicare Povidone-Iodine Scrub

Product NDC
52380-0024
Requested package NDC
52380-0024-3
11-digit product format
523800024
Labeler code
52380
Product ID
52380-0024_efe34b32-3be4-cf93-e053-2a95a90ab385
Type
HUMAN OTC DRUG
Nonproprietary name
Povidone-iodine Scrub
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Aplicare Products, LLC
Application
part333A
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
1992-07-01
Marketing end
2025-03-31
Substance
POVIDONE-IODINE
Active strength
10 mg/mL
NDC exclude flag
No
Listing certified through
0000-00-00
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage52380-002452380-0024-3DDiscontinued by firm2026-10-05

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, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
52380-0024-1EA - Each52380-0024843ed340-2493-4895-a8e0-c7c35869bae112012-07-24
52380-0024-2EA - Each52380-00245488a2ec-58b8-482f-a4c8-9b64dc53c44212012-07-24
52380-0024-3EA - Each52380-00246eec9b6a-a324-4e25-b794-9d52f8e83b1412012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99MAPLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
IODINEACTIVE MOIETY9679TC07X4APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
AMMONIUM NONOXYNOL-4 SULFATEINACTIVE INGREDIENT9HIA70O4J0APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLAPLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9TAPLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IAPLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
SODIUM PHOSPHATE, DIBASICINACTIVE INGREDIENTGR686LBA74APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RAPLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE SCRUB) SOLUTION [APLICARE, INC.]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52380-0024-352380002403120 mL in 1 PACKET (52380-0024-3) 120 ml1992-07-012025-01-31NoNoCurrent