Provodine

Product NDC
59426-001
11-digit product format
594260001
Labeler code
59426
Product ID
59426-001_e771a266-8743-4a45-87e3-ea88acf2e9cb
Type
HUMAN OTC DRUG
Nonproprietary name
providone iodine
Dosage form
EMULSION
Route
TOPICAL
Labeler
Microdermis Corporation
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-09-15
Marketing end
0000-00-00
Substance
POVIDONE-IODINE
Active strength
8 mg/mL
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct59426-001IInactivated by FDA2026-07-31
excluded packagepackage59426-00159426-001-03IInactivated by FDA2026-07-31
excluded packagepackage59426-00159426-001-04IInactivated by FDA2026-07-31
excluded packagepackage59426-00159426-001-16IInactivated by FDA2026-07-31

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5f30b278-5791-4113-8781-878a9221ef8aProduct name220230125
2a70c781-a755-4d76-b20a-a958acfbdcdcProduct name220190619
304592ef-4a8a-4c22-8e8c-af73aa3d60e5Product name120180703
ac0821a1-ce75-4ea7-880a-59eecaecdf22Product name120180703
db5dc4f9-b907-46f6-8fb7-babcf04bbe5cProduct name120180619
41e9d6cf-3ed7-4c44-a57e-0685058d0896Product name120170824
5e652c92-68fd-426b-b0e7-5fc64e0b9f99Product name120170309
ddc0c11a-bba8-408f-b3c7-c4828b4bcc8cProduct name120150421

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59426-001-032020-01-31C16284748780-19d75b9d0-1b16-f424-e053-dadaa90a57ceProvodine
59426-001-042020-01-31C16284748780-19d75b9d0-1b16-f424-e053-dadaa90a57ceProvodine
59426-001-162020-01-31C16284748780-19d75b9d0-1b16-f424-e053-dadaa90a57ceProvodine

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59426-001-03Provodine3 mL in 1 PACKETEMULSION34
59426-001-03Provodine100 in 1 BOXEMULSION1004
59426-001-04Provodine118 mL in 1 BOTTLEEMULSION1184
59426-001-16Provodine473 mL in 1 BOTTLEEMULSION4734

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
POVIDONE-IODINEACTIVE INGREDIENT85H0HZU99MPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
IODINEACTIVE MOIETY9679TC07X4PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
ALLANTOININACTIVE INGREDIENT344S277G0ZPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W7PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
BETASIZOFIRANINACTIVE INGREDIENT2X51AD1X3TPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RAPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
C13-14 ISOPARAFFININACTIVE INGREDIENTE4F12ROE70PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
CETYL ALCOHOLINACTIVE INGREDIENT936JST6JCNPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
DISTEARYLDIMONIUM CHLORIDEINACTIVE INGREDIENTOM9573ZX3XPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86KPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
GLYCERYL LAURATEINACTIVE INGREDIENTY98611C087PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
GLYCERYL MONOSTEARATEINACTIVE INGREDIENT230OU9XXE4PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
LAURETH-7INACTIVE INGREDIENTZ95S6G8201PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
MEDIUM-CHAIN TRIGLYCERIDESINACTIVE INGREDIENTC9H2L21V7UPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
NONOXYNOL-9INACTIVE INGREDIENT48Q180SH9TPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
OCTOXYNOL-9INACTIVE INGREDIENT7JPC6Y25QSPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
PEG-100 STEARATEINACTIVE INGREDIENTYD01N1999RPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
PIDOLIC ACIDINACTIVE INGREDIENTSZB83O1W42PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
POLYACRYLAMIDE (10000 MW)INACTIVE INGREDIENTE2KR9C9V2IPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
POLYGLYCERYL-3 DIISOSTEARATEINACTIVE INGREDIENT46P231IQV8PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)INACTIVE INGREDIENT0L414VCS5YPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
WATERINACTIVE INGREDIENT059QF0KO0RPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4
YELLOW WAXINACTIVE INGREDIENT2ZA36H0S2VPROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59426-001PROVODINE (PROVIDONE IODINE) EMULSION [MICRODERMIS CORPORATION]4Legacy NDC, 4 package rows20150703_6819df87-aaf8-49f8-a95d-acb6926d6848.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
59426-001-03594260001033 mL in 1 PACKET3 mlHistorical
59426-001-0459426000104118 mL in 1 BOTTLE118 mlHistorical
59426-001-1659426000116473 mL in 1 BOTTLE473 mlHistorical