Loris Povidone-Iodine

Product NDC
68356-119
Requested package NDC
68356-119-01
11-digit product format
683560119
Labeler code
68356
Product ID
68356-119_e9bdeac8-1bf5-b510-e053-2a95a90a089c
Type
HUMAN OTC DRUG
Nonproprietary name
Povidone-Iodine
Dosage form
LIQUID
Route
TOPICAL
Labeler
LernaPharm Loris Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2013-04-13
Marketing end
0000-00-00
Substance
POVIDONE-IODINE
Active strength
1 g/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage68356-11968356-119-01DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68356-119LORIS POVIDONE-IODINE SOLUTION (POVIDONE-IODINE) LIQUID [LERNAPHARM LORIS INC.]8Legacy NDC20231022_7a1ba66a-e5be-415f-8aee-c132330836d4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68356-119-01683560119013 APPLICATOR in 1 POUCH (68356-119-01) > 2.5 mL in 1 APPLICATOR3 applicator2013-04-160000-00-00NoNoCurrent