Advanced Antiseptic

Product NDC
41190-210
11-digit product format
411900210
Labeler code
41190
Product ID
41190-210_817df8af-f419-49fd-9370-3bcc649e72f7
Type
HUMAN OTC DRUG
Nonproprietary name
Eucalyptol
Dosage form
MOUTHWASH
Route
ORAL
Labeler
Wakefern Food Corporation
Application
part356
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-11-24
Marketing end
0000-00-00
Substance
EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Active strength
0 mL/100L; mL/100L; mL/100L; mL/100L
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#