menthol cough drops
- Product NDC
- 10202-020
- Requested package NDC
- 10202-020-40
- 11-digit product format
- 102020020
- Labeler code
- 10202
- Product ID
- 10202-020_ed9b2d6f-a0ee-179e-e053-2a95a90ad046
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- menthol
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- 7-Eleven Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-07-28
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 10202-020 | 10202-020-40 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 10202-020-40 | 10202002040 | 40 LOZENGE in 1 BAG (10202-020-40) | 40 lozenge | 2016-07-28 | 0000-00-00 | No | No | Current |