MENTHOL
- Product NDC
- 80465-002
- 11-digit product format
- 804650002
- Labeler code
- 80465
- Product ID
- 80465-002_e2881878-f26a-84e9-e053-2a95a90a24cb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- LIQUID
- Route
- NASAL
- Labeler
- EROS GLOBAL CORP
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-09-21
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 2 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80465-002-04 | 80465000204 | 113 g in 1 BOTTLE (80465-002-04) | 113 g | 2020-09-21 | 0000-00-00 | No | No | Current |