FDA.reportPublic FDA data

KROGER

Product NDC
30142-519
11-digit product format
301420519
Labeler code
30142
Product ID
30142-519_f4cb5ad5-c8d8-4c81-a08e-443c00b6178d
Type
HUMAN OTC DRUG
Nonproprietary name
SELENIUM SULFIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
THE KROGER COMPANY
Application
part358H
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-06-24
Marketing end
0000-00-00
Substance
SELENIUM SULFIDE
Active strength
10 mg/mL
NDC exclude flag
No
Listing certified through
2019-12-31
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.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct30142-519IInactivated by FDA2026-07-31
excluded packagepackage30142-51930142-519-11IInactivated by FDA2026-07-31

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MG217 Psoriasis Therapeutic Scalp TreatmentCOAL TARWisconsin Pharmacal Company6d3f4685-eb47-445e-86fb-3601d2c110e72018-12-10WarningsExact identifier
MG217 Psoriasis Medicated ConditioningCOAL TARWisconsin Pharmacal Company7cafb511-0ab7-f3b4-e053-2991aa0a2e0b2018-12-10WarningsExact identifier
Overnight ClearingSALICYLIC ACIDDermalogica, Inc.6f6d9bd9-a1c8-4f8c-b7b8-fe9748a06c2c2017-12-04WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

Warnings For external use only. Ask doctor before use if condition covers a large area of the body. When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water. use caution in exposing skin to sunlight. It may increase your tendency to sunburn for up to 24 hours after application. do not use with other forms of psoriasis therapy such as ultraviolet radiation or prescription drugs unless directed by a physician. do not use for prolonged periods without consulting a physician. Stop use and ask a doctor if condition worsens. condition does not improve after regular use of this product as directed. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately. WARNING This product can gose you to chemicals including Coal Tar, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
30142-519-112020-01-31C16284748780-19d75b9d0-f778-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
30142-519-11KROGERMEDICATED DANDRUFF325 mL in 1 BOTTLE, PLASTICLIQUID3251

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SELENIUM SULFIDEACTIVE INGREDIENTZ69D9E381QKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
SELENIUM SULFIDEACTIVE MOIETYZ69D9E381QKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
AMMONIUM CHLORIDEINACTIVE INGREDIENT01Q9PC255DKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
COCAMIDOPROPYL BETAINEINACTIVE INGREDIENT5OCF3O11KXKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
D&C RED NO. 33INACTIVE INGREDIENT9DBA0SBB0LKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
DMDM HYDANTOININACTIVE INGREDIENTBYR0546TOWKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
MAGNESIUM ALUMINUM SILICATEINACTIVE INGREDIENT6M3P64V0NCKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
MENTHOLINACTIVE INGREDIENTL7T10EIP3AKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)INACTIVE INGREDIENT74G4R6TH13KROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
SODIUM LAURETH SULFATEINACTIVE INGREDIENTBPV390UAP0KROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
TEA-LAURYL SULFATEINACTIVE INGREDIENTE8458C1KAAKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1
WATERINACTIVE INGREDIENT059QF0KO0RKROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
30142-519KROGER MEDICATED DANDRUFF (SELENIUM SULFIDE) LIQUID [THE KROGER COMPANY]1Legacy NDC, 1 package rows20140626_e156c967-a8b1-4755-ad5b-cd5008695494.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
204642selenium sulfide 1 % Medicated ShampooPSNe156c967-a8b1-4755-ad5b-cd50086954941
204642selenium sulfide 10 MG/ML Medicated ShampooSCDe156c967-a8b1-4755-ad5b-cd50086954941
204642selenium sulfide 1 % Lotion ShampooSYe156c967-a8b1-4755-ad5b-cd50086954941
204642selenium sulfide 1 % Medicated ShampooSYe156c967-a8b1-4755-ad5b-cd50086954941

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
30142-519-1130142051911325 mL in 1 BOTTLE, PLASTIC325 mlHistorical