Home NDC 68605-2010 END-ZIT
Product NDC 68605-2010
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 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 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 68605-2010-2 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 68605-2010-2 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 68605-2010-2 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 68605-2010-2 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 68605-2010-2 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 68605-2010-2 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 68605-2010-2 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 68605-2010-2 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 68605-2010-2 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 68605-2010-2 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 68605-2010-2 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 68605-2010-2 557ba5c1ecfa…9c80585c8c6e…
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68605-2010-2 END-ZIT 70 g in 1 TUBE LOTION, AUGMENTED 70 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 68605-2010 END-ZIT (SULFUR) LOTION, AUGMENTED [ABBE LABORATORIES, INC.] 7 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 1 of 1 · 1 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 68605-2010-2 68605201002 70 g in 1 TUBE (68605-2010-2) 70 g 2004-04-20 0000-00-00 No No Current