Home NDC 52380-1738-5 Aplicare Povidone Iodine
Product NDC 52380-1738
Requested package NDC 52380-1738-5
11-digit product format 523801738
Labeler code 52380
Product ID 52380-1738_d2195149-8a70-1445-e053-2995a90aec96
Type HUMAN OTC DRUG
Nonproprietary name Povidone Iodine
Dosage form GEL
Route TOPICAL
Labeler Aplicare Products, LLC
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 1998-09-01
Marketing end 2022-11-06
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 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded POVIDONE-IODINE ACTIVE INGREDIENT 85H0HZU99M APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 IODINE ACTIVE MOIETY 9679TC07X4 APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 DIMETHICONE INACTIVE INGREDIENT 92RU3N3Y1O APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) INACTIVE INGREDIENT S38J6RZN16 APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 NONOXYNOL-10 INACTIVE INGREDIENT K7O76887AP APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 SODIUM PHOSPHATE, DIBASIC ANHYDROUS INACTIVE INGREDIENT 22ADO53M6F APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4 WATER INACTIVE INGREDIENT 059QF0KO0R APLICARE POVIDONE IODINE (POVIDONE IODINE) GEL [APLICARE, INC.] 4
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52380-1738-5 52380173805 118 mL in 1 BOTTLE (52380-1738-5) 118 ml 1998-09-01 2022-11-06 No No Current