Menthol
- Product NDC
- 63940-014
- 11-digit product format
- 639400014
- Labeler code
- 63940
- Product ID
- 63940-014_c77cdca9-e14a-5892-e053-2a95a90af38f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Maximum Strength Medicated Foot Powder
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Harmon Store Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-02-18
- 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
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 63940-014 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 63940-014 | 63940-014-10 | D | Discontinued by firm | | 2026-07-31 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63940-014-10 | 63940001410 | 283 g in 1 BOTTLE, PLASTIC (63940-014-10) | 283 g | 2014-02-18 | 0000-00-00 | No | No | Current |