Home NDC 68605-2002 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 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/g
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 68605-2002-2 END-ZIT 17.57 g in 1 BOTTLE, GLASS LOTION, AUGMENTED 17.57 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 68605-2002 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 13 of 55 · 1,088 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Oil Free Acne Wash SALICYLIC ACID 2% CVS Pharmacy, Inc. 7a8225ab-b60a-4978-bdfe-db0b00307ef1 2026-02-03 Warnings Exact identifier application number: M006 Acne Treatment BENZOYL PEROXIDE CVS Pharmacy, Inc. d9fbaeba-cebf-4d02-aa7d-3ee1d2fdc50c 2026-02-02 Warnings, Adverse reactions Exact identifier application number: M006 Even and Clear Exfoliating Wash SALICYLIC ACID Ambi Enterprises, LLC 499d7616-4677-f6a7-e063-6294a90aeaa2 2026-01-30 Warnings Exact identifier application number: M006 Medicated Apricot Scrub SALICYLIC ACID Rite Aid Corporation fb90b880-07e5-4bda-b907-228a66950555 2026-01-30 Warnings, Adverse reactions Exact identifier application number: M006 Acne Treatment BENZOYL PEROXIDE Rite Aid Corporation a51b7668-1ba1-42cb-b804-4fdf76610695 2026-01-30 Warnings, Adverse reactions Exact identifier application number: M006 Acne Treatment SALICYLIC ACID Natureplex, LLC 31b50718-cc60-460d-aad7-b9620970d411 2026-01-29 Warnings Exact identifier application number: M006 Peace Out Acne Cleanser SALICYLIC ACID Peace Out LLC 0a8897b0-cb8f-ba50-e063-6394a90a7f34 2026-01-29 Warnings Exact identifier application number: M006 Peace Out Acne Moisturizer SALICYLIC ACID Peace Out LLC. 18bb4314-0b18-b3bc-e063-6294a90a1854 2026-01-29 Warnings Exact identifier application number: M006 ZITFREE ACNE TREATMENT BENZOYL PEROXIDE Natureplex, LLC 70c2e3fb-e643-467b-80fd-c40e3c3e9513 2026-01-29 Warnings Exact identifier application number: M006 ProBliva Antibacterial and Acne Body Wash ANTIBACTERIAL AND ACNE BODY WASH CAVTECH HOLDING LLC 496f7a1e-05b6-d434-e063-6394a90afe54 2026-01-28 Warnings Exact identifier application number: M006 Sunscreen SPF50 NON NANO ZINC OXIDE SBS BILIMSEL BIO COZUMLER SANAYI VE TICARET ANONIM SIRKETI PINAR SUBESI c5d52f13-a649-9579-e053-2a95a90a062c 2026-01-27 Warnings Exact identifier application number: M006 Viaderma Calm Anti-Itch HYDROCORTISONE VIADERMA DISTRIBUTION INC ea281bde-a7a2-47b6-895a-5dc2924972de 2026-01-27 Warnings Exact identifier application number: M006 Viaderma Clear Acne Treatment SALICYLIC ACID VIADERMA DISTRIBUTION INC ace405bd-6fe6-4db1-ba1f-9b9861abe663 2026-01-27 Warnings Exact identifier application number: M006 DHC Acne Spot Therapy SULFUR DHC USA Incorporated 84d49048-95cf-4f14-9698-c746237fec9d 2026-01-24 Warnings Exact identifier application number: M006 MEDPURA Benzoyl Peroxide Aqueous Base, Acne Treatment Gel BENZOYL PEROXIDE Akron Pharma Inc. b7d335d1-3022-4b28-913c-477152a7dad2 2026-01-23 Warnings Exact identifier application number: M006 Skinkure Acne Eraser Spot Treatment SALICYLIC ACID SKINKURE, LLC 0fc85727-4321-7750-e063-6294a90ad3fe 2026-01-23 Warnings Exact identifier application number: M006 Emuaid SALICYLIC ACID Speer Laboratories, LLC a1486276-30f7-4245-815b-d57edf411cda 2026-01-23 Warnings Exact identifier application number: M006 Neutrogena Evenly Clear Acne Cleanser SALICYLIC ACID Kenvue Brands LLC 3e985a61-2aa7-963b-e063-6294a90a7c12 2026-01-22 Warnings Exact identifier application number: M006 Resurfacing acne swipes SALICYLIC ACID SKIN PS Brands 9629fdcb-f3b5-9685-e053-2a95a90a0230 2026-01-22 Warnings Exact identifier application number: M006 PanOxyl SALICYLIC ACID Crown Laboratories 48fd0106-4db4-f33a-e063-6294a90a5a0b 2026-01-22 Warnings Exact identifier application number: M006
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 68605-2002-2 68605200202 17.57 g in 1 BOTTLE, GLASS (68605-2002-2) 17.57 g 2004-04-20 0000-00-00 No No Current