FDA.reportPublic FDA data

END-ZIT

Product NDC
68605-2002
11-digit product format
686052002
Labeler code
68605
Product ID
68605-2002_9a07e62f-1c38-4055-b5ae-b1c06d08dd69
Type
HUMAN OTC DRUG
Nonproprietary name
SULFUR
Dosage form
LOTION, AUGMENTED
Route
TOPICAL
Labeler
ABBE Laboratories, Inc.
Application
M006
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2004-04-20
Substance
SULFUR
Active strength
.05 g/g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
END-ZIT
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR.05 g/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii70FD1KFU70
Rxcui422938, 1094323

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68605-2002-2END-ZIT17.57 g in 1 BOTTLE, GLASSLOTION, AUGMENTED17.579

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
68605-2002END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.]7Current NDC, Legacy NDC, 1 package rows20231102_afed5e8e-324c-44c6-abf6-72938376a4b2.zip

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
68605-2002-26860520020217.57 g in 1 BOTTLE, GLASS (68605-2002-2) 17.57 g2004-04-200000-00-00NoNoCurrent