Eugenol
- Product NDC
- 61291-011
- 11-digit product format
- 612910011
- Labeler code
- 61291
- Product ID
- 61291-011_0f0b6a1c-be77-40b6-b7be-2209f873891a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eugenol
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Polysciences, Inc
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-01-30
- Marketing end
- 0000-00-00
- Substance
- EUGENOL
- Active strength
- 850 mg/mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record