Home NDC 68605-2001 END-ZIT
Product NDC 68605-2001
11-digit product format 686052001
Labeler code 68605
Product ID 68605-2001_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/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base END-ZIT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR .05 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 422938 Internal RxNorm lookup 1094323 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68605-2001-2 END-ZIT 14.78 mL in 1 BOTTLE, GLASS LOTION, AUGMENTED 14.78 9
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SULFUR ACTIVE INGREDIENT 70FD1KFU70 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 SULFUR ACTIVE MOIETY 70FD1KFU70 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 CAMPHOR (SYNTHETIC) INACTIVE INGREDIENT 5TJD82A1ET END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 DIAZOLIDINYL UREA INACTIVE INGREDIENT H5RIZ3MPW4 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 ISOPROPYL ALCOHOL INACTIVE INGREDIENT ND2M416302 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 SODIUM LAURETH SULFATE INACTIVE INGREDIENT BPV390UAP0 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 TALC INACTIVE INGREDIENT 7SEV7J4R1U END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 WATER INACTIVE INGREDIENT 059QF0KO0R END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2 ZINC OXIDE INACTIVE INGREDIENT SOI2LOH54Z END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68605-2001 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 7 Current NDC, Legacy NDC, 1 package rows 20231102_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 42 of 55 · 1,088 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68605-2001-2 68605200102 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2) 14.78 ml 2004-04-20 0000-00-00 No No Current