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 38 of 55 · 1,088 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join TREAT SO DEEP ACNE-FIGHTING TREATMENT SALICYLIC ACID ASPIRE BRANDS INC d18b4f15-9ea1-4d76-a1e3-a0be1c5bb58a 2024-12-06 Warnings Exact identifier application number: M006 Oxy Maximum Strength Rapid Spot Treatment OXY MAXIMUM STRENGTH RAPID SPOT TREATMENT The Mentholatum Company 28886273-a71a-46ea-e063-6394a90ac11d 2024-12-05 Warnings Exact identifier application number: M006 Dermaclear Spot Treatment BENZOYL PEROXIDE Allure Labs Inc 45a93c47-552f-4660-a37c-7a8cceac2d8e 2024-12-05 Warnings Exact identifier application number: M006 DermaClear Pads SALICYLIC ACID Allure Labs 0c6624fd-88f9-402c-8ac2-bc278242b484 2024-12-05 Warnings Exact identifier application number: M006 DermaClear BHA Spot Treatment SALICYLIC ACID Allure Labs b629cb05-548e-4d60-e053-2a95a90aeefb 2024-12-05 Warnings Exact identifier application number: M006 Acne Treatment Maximum Strength SALICYLIC ACID Young Living Essential Oils, LC 756a52ff-161d-4b6e-933b-49bce885d998 2024-12-04 Warnings Exact identifier application number: M006 DermaClear Serum SALICYLIC ACID Allure Labs Inc 487a7d1c-0f98-4d36-bfe9-c12bcda8d0b3 2024-12-04 Warnings Exact identifier application number: M006 Dermaclear Mask SALICYLIC ACID Allure Labs Inc, 9429f477-a916-49c9-bf04-1cf591af5c7f 2024-12-04 Warnings Exact identifier application number: M006 Clear System Clarifying Gel Cleanser SALICYLIC ACID Bentley Laboratories, LLC 08248e40-aa71-4dfb-8a75-af8886ccb976 2024-12-04 Warnings Exact identifier application number: M006 DermaClear BHA Cleanser SALICYLIC ACID Allure Labs Inc bfeced33-a630-4f1d-9ecf-33450bd26ae9 2024-12-03 Warnings Exact identifier application number: M006 PCA SKIN Intensive Clarity Treatment SALICYLIC ACID CP Skin Health Group, Inc. 7bd6edc0-941e-492d-8b3c-4e8b3425f929 2024-12-03 Warnings Exact identifier application number: M006 PCA SKIN BPO Cleanser BENZOYL PEROXIDE CP Skin Health Group, Inc. eb55cc26-cf47-4e9e-b7a8-23ef82aecce2 2024-12-03 Warnings Exact identifier application number: M006 PCA SKIN Acne BENZOYL PEROZIDE CP Skin Health Group, Inc. 257bd9dd-93f9-4996-8478-8198be3ef683 2024-12-03 Warnings Exact identifier application number: M006 PCA Gel SALICYLIC ACID CP Skin Health Group, Inc 396b4675-451f-48b2-b139-19508434e0fe 2024-12-03 Warnings Exact identifier application number: M006 CliniCalm HYDROCORTISONE CP Skin Health Group, Inc. febcf7e8-668c-a5c9-e053-6394a90aec39 2024-12-03 Warnings Exact identifier application number: M006 Alumier MD Acne Clarifying Cleanser SALICYLIC ACID Alumier Labs 87747f82-9018-ab34-e053-2995a90a6808 2024-12-01 Warnings Exact identifier application number: M006 Acne Control Face Wash SALICYLIC ACID Bentley Laboratories, LLC 068c5fef-cdc5-49f4-9372-9cfdd07508b8 2024-11-28 Warnings Exact identifier application number: M006 Acne Control Body Wash SALICYLIC ACID Bentley Laboratories, LLC 3db0f885-4c08-4678-8533-ba2025bf7d48 2024-11-28 Warnings Exact identifier application number: M006 Neutrogena Stubborn Blackheads Daily Serum SALICYLIC ACID Kenvue Brands LLC c0992ceb-5f7a-4c8f-a43f-7a300bd6bbf1 2024-11-26 Warnings Exact identifier application number: M006 Neutrogena Stubborn Acne Spot Drying SULFUR Kenvue Brands LLC dffe9bf4-a8a2-4fa0-e053-2995a90abcb3 2024-11-26 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