RITE AID RENEWAL

Product NDC
11822-6211
11-digit product format
118226211
Labeler code
11822
Product ID
11822-6211_ff89aadc-d3ad-4982-9f21-6d1b6472eec3
Type
HUMAN OTC DRUG
Nonproprietary name
SELENIUM SULFIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
RITE AID CORPORATION
Application
part358H
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2013-06-20
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 productproduct11822-6211IInactivated by FDA2026-07-31
excluded packagepackage11822-621111822-6211-1IInactivated 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
11822-6211-12020-01-31C16284748780-19d75b9d1-19e6-f424-e053-dadaa90a57ceDRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-6211-1RITE AID RENEWAL325 mL in 1 BOTTLE, PLASTICLIQUID3251

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SELENIUM SULFIDEACTIVE INGREDIENTZ69D9E381QRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
SELENIUM SULFIDEACTIVE MOIETYZ69D9E381QRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
ALOE VERA LEAFINACTIVE INGREDIENTZY81Z83H0XRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
COCAMIDOPROPYL BETAINEINACTIVE INGREDIENT5OCF3O11KXRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
DIHYDROGENATED TALLOW PHTHALIC ACID AMIDEINACTIVE INGREDIENT1R81RPY10GRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1ORITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
DMDM HYDANTOININACTIVE INGREDIENTBYR0546TOWRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WORITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULRRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
SODIUM LAURETH SULFATEINACTIVE INGREDIENTBPV390UAP0RITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
SODIUM STEAROYL LACTYLATEINACTIVE INGREDIENTIN99IT31LNRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1
WATERINACTIVE INGREDIENT059QF0KO0RRITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-6211RITE AID RENEWAL (SELENIUM SULFIDE) LIQUID [RITE AID CORPORATION]1Legacy NDC, 1 package rows20130624_b1482958-8370-43fc-8789-0f329bfe676a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
204642selenium sulfide 1 % Medicated ShampooPSNb1482958-8370-43fc-8789-0f329bfe676a1
204642selenium sulfide 10 MG/ML Medicated ShampooSCDb1482958-8370-43fc-8789-0f329bfe676a1
204642selenium sulfide 1 % Lotion ShampooSYb1482958-8370-43fc-8789-0f329bfe676a1
204642selenium sulfide 1 % Medicated ShampooSYb1482958-8370-43fc-8789-0f329bfe676a1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
11822-6211-111822621101325 mL in 1 BOTTLE, PLASTIC325 mlHistorical