Antiseptic
- Product NDC
- 51143-210
- 11-digit product format
- 511430210
- Labeler code
- 51143
- Product ID
- 51143-210_31651900-c5ae-4827-a592-8ad685d25dc2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eucalyptol
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Onpoint, Inc
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-10-19
- 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#