Home NDC 68776-1001-2 Wyandotte Sanifect E3
Product NDC 68776-1001
Requested package NDC 68776-1001-2
11-digit product format 687761001
Labeler code 68776
Product ID 68776-1001_0d89392b-f8e2-4b42-b652-63dd1259a336
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form LOTION
Route TOPICAL
Labeler Alex C. Fergusson, Inc.
Application part333E
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2006-10-01
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 60 L/100L
NDC exclude flag No
Listing certified through 2020-12-31
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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 68776-1001 68776-1001-2 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68776-1001 WYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ACUITY SPECIALTY PRODUCTS, INC DBA AFCO US] 6 Legacy NDC 20241220_8b22eb07-af79-410a-bdc8-872899928f63.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68776-1001-2 68776100102 208 L in 1 DRUM (68776-1001-2) 208 l 2006-10-01 0000-00-00 No No Current