Menthol
- Product NDC
- 11673-511
- 11-digit product format
- 116730511
- Labeler code
- 11673
- Product ID
- 11673-511_c79376de-009e-0e7c-e053-2995a90a3677
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Maximum Strength Medicated Foot Powder Talc Free
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Target Corporation
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-11-27
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 3 g/283g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-511 | MENTHOL (MAXIMUM STRENGTH MEDICATED FOOT POWDER TALC FREE) POWDER [TARGET CORPORATION] | 6 | Legacy NDC | 20241213_cee20e8e-3a44-437b-83ef-0f5303fece2a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-511-10 | 11673051110 | 283 g in 1 BOTTLE, PLASTIC (11673-511-10) | 283 g | 2017-11-27 | 0000-00-00 | No | No | Current |