Appeal Alcohol Foaming Hand Sanitizer

Product NDC
11084-702
11-digit product format
110840702
Labeler code
11084
Product ID
11084-702_9dedfc3e-92be-447b-b627-f4855dd662f2
Type
HUMAN OTC DRUG
Nonproprietary name
Ethyl Alcohol
Dosage form
LIQUID
Route
TOPICAL
Labeler
SC Johnson Professional USA, Inc.
Application
part333E
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2012-05-15
Marketing end
0000-00-00
Substance
ALCOHOL
Active strength
70 mL/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct11084-702DDiscontinued by firm2026-10-05
excluded packagepackage11084-70211084-702-27DDiscontinued by firm2026-10-05

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
NDCDashboard titleSPL versionValidationDashboard ZIP
11084-702APPEAL ALCOHOL FOAMING HAND SANITIZER (ETHYL ALCOHOL) LIQUID [SC JOHNSON PROFESSIONAL USA, INC.]7Legacy NDC20241218_6b35e9f7-1e3e-41c6-9250-e1ce744b302e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11084-702-27110840702271000 mL in 1 BOTTLE, PLASTIC (11084-702-27) 1000 ml2012-05-150000-00-00NoNoCurrent