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#