FDA.reportPublic FDA data

Wyandotte Sanifect E3

Product NDC
68776-1001
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct68776-1001DDiscontinued by firm2026-10-05
excluded packagepackage68776-100168776-1001-1DDiscontinued by firm2026-10-05
excluded packagepackage68776-100168776-1001-2DDiscontinued by firm2026-10-05

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 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct68776-1001DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage68776-100168776-1001-2DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage68776-100168776-1001-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90MWYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2
ALCOHOLACTIVE MOIETY3K9958V90MWYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2
AMINOMETHYLPROPANOLINACTIVE INGREDIENTLU49E6626QWYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2
CARBOMER HOMOPOLYMER TYPE CINACTIVE INGREDIENT4Q93RCW27EWYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2
GLYCERININACTIVE INGREDIENTPDC6A3C0OXWYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302WYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RWYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ALEX C. FERGUSSON, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68776-1001WYANDOTTE SANIFECT E3 (ALCOHOL) LOTION [ACUITY SPECIALTY PRODUCTS, INC DBA AFCO US]6Legacy NDC20241220_8b22eb07-af79-410a-bdc8-872899928f63.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68776-1001-1687761001013.784 L in 1 BOTTLE (68776-1001-1) 3.784 l2006-10-010000-00-00NoNoCurrent
68776-1001-268776100102208 L in 1 DRUM (68776-1001-2) 208 l2006-10-010000-00-00NoNoCurrent