FDA.reportPublic FDA data

END-ZIT

Product NDC
68605-2010
Requested package NDC
68605-2010-2
11-digit product format
686052010
Labeler code
68605
Product ID
68605-2010_6bcf04bf-f9bd-48a6-9fe6-5d1049326347
Type
HUMAN OTC DRUG
Nonproprietary name
SULFUR
Dosage form
LOTION, AUGMENTED
Route
TOPICAL
Labeler
ABBE Laboratories, Inc.
Application
part333D
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2004-04-20
Marketing end
0000-00-00
Substance
SULFUR
Active strength
0 g/g
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 packagepackage68605-201068605-2010-2DDiscontinued by firm2026-10-05

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 dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68605-2010-2END-ZIT70 g in 1 TUBELOTION, AUGMENTED709

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SULFURACTIVE INGREDIENT70FD1KFU70END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
SULFURACTIVE MOIETY70FD1KFU70END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
CAMPHOR (SYNTHETIC)INACTIVE INGREDIENT5TJD82A1ETEND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
DIAZOLIDINYL UREAINACTIVE INGREDIENTH5RIZ3MPW4END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TEND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHEND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
SODIUM LAURETH SULFATEINACTIVE INGREDIENTBPV390UAP0END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
TALCINACTIVE INGREDIENT7SEV7J4R1UEND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPEND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
WATERINACTIVE INGREDIENT059QF0KO0REND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2
ZINC OXIDEINACTIVE INGREDIENTSOI2LOH54ZEND-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68605-2010END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]7Legacy NDC, 1 package rows20231102_afed5e8e-324c-44c6-abf6-72938376a4b2.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
END-ZITSULFURABBE Laboratories, Inc.afed5e8e-324c-44c6-abf6-72938376a4b22026-01-13WarningsExact identifier
ndc (package): 68605-2010-2
ndc (product): 68605-2010
ndc11 (package): 68605201002

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1094323End-Zit 5 % Topical LotionPSNafed5e8e-324c-44c6-abf6-72938376a4b29
422938sulfur 5 % Topical LotionPSNafed5e8e-324c-44c6-abf6-72938376a4b29
1094323sulfur 50 MG/ML Topical Lotion [End-Zit]SBDafed5e8e-324c-44c6-abf6-72938376a4b29
422938sulfur 50 MG/ML Topical LotionSCDafed5e8e-324c-44c6-abf6-72938376a4b29
1094323End-Zit 5 % Topical LotionSYafed5e8e-324c-44c6-abf6-72938376a4b29
1094323End-Zit 50 MG/ML Topical LotionSYafed5e8e-324c-44c6-abf6-72938376a4b29
422938sulfur 5 % Topical LotionSYafed5e8e-324c-44c6-abf6-72938376a4b29

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68605-2010-26860520100270 g in 1 TUBE (68605-2010-2) 70 g2004-04-200000-00-00NoNoCurrent