Advanced Antiseptic

Product NDC
53942-210
11-digit product format
539420210
Labeler code
53942
Product ID
53942-210_427c19eb-33e6-4943-a48d-c2b803e0d8eb
Type
HUMAN OTC DRUG
Nonproprietary name
Eucalyptol
Dosage form
MOUTHWASH
Route
ORAL
Labeler
Demoulas Super Markets, Inc
Application
part348
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-07-22
Marketing end
0000-00-00
Substance
EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Active strength
0 kg/100L; kg/100L; kg/100L; kg/100L
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
53942-210-862025-02-20C16284748780-19d75b9cf-f85d-f424-e053-dadaa90a57cedb61a617-849e-45e8-940b-3b39ddf78209
53942-210-862020-01-31C16284748780-19d75b9cf-f85d-f424-e053-dadaa90a57cedb61a617-849e-45e8-940b-3b39ddf78209