Home NDC 52380-4802 Aplicare Povidone-iodine Scrub
Product NDC 52380-4802
11-digit product format 523804802
Labeler code 52380
Product ID 52380-4802_5a8748b6-17b0-cdca-e063-6394a90ad140
Type HUMAN OTC DRUG
Nonproprietary name Povidone-iodine
Dosage form SOLUTION
Route TOPICAL
Labeler Aplicare Products, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 1998-01-01
Substance POVIDONE-IODINE
Active strength 7.5 mg/mL
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 · 2 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 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product 52380-4802 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 52380-4802 52380-4802-8 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…
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 Aplicare Povidone-iodine Scrub
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POVIDONE-IODINE 7.5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 85H0HZU99M Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 314188 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 52380-4802-8 Aplicare Povidone-iodine Scrub 118 mL in 1 BOTTLE, PLASTIC SOLUTION 118 14
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POVIDONE-IODINE ACTIVE INGREDIENT 85H0HZU99M APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 IODINE ACTIVE MOIETY 9679TC07X4 APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 AMMONIUM NONOXYNOL-4 SULFATE INACTIVE INGREDIENT 9HIA70O4J0 APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 ANHYDROUS CITRIC ACID INACTIVE INGREDIENT XF417D3PSL APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 NONOXYNOL-9 INACTIVE INGREDIENT 48Q180SH9T APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 SODIUM PHOSPHATE, DIBASIC INACTIVE INGREDIENT GR686LBA74 APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6 WATER INACTIVE INGREDIENT 059QF0KO0R APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE, INC.] 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52380-4802 APLICARE POVIDONE-IODINE SCRUB (POVIDONE-IODINE) SOLUTION [APLICARE PRODUCTS, LLC] 13 Current NDC, Legacy NDC, 1 package rows 20240110_b8a23a29-2541-4987-a534-17a6369a6c8d.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 1 of 1 · 1 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 52380-4802-8 52380480208 118 mL in 1 BOTTLE, PLASTIC (52380-4802-8) 118 ml 1998-01-01 0000-00-00 No No Current