Listerine Antiseptic
- Product NDC
- 42002-401
- 11-digit product format
- 420020401
- Labeler code
- 42002
- Product ID
- 42002-401_5514d206-f86c-48c0-998f-0251118c10e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eucalyptol, Menthol, Methyl Salicylate, and Thymol
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Johnson & Johnson Consumer Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-03-01
- Marketing end
- 2020-12-10
- Substance
- EUCALYPTOL; MENTHOL, UNSPECIFIED FORM; METHYL SALICYLATE; THYMOL
- Active strength
- 1 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#