Cherry Cough Drop
- Product NDC
- 52642-012
- 11-digit product format
- 526420012
- Labeler code
- 52642
- Product ID
- 52642-012_edc3f507-cce7-2e27-e053-2995a90a139b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- BestCo Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2015-04-27
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 6 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 product | product | 52642-012 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 52642-012 | 52642-012-00 | D | Discontinued by firm | 2026-10-05 |
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 |
|---|---|---|---|---|---|---|---|---|
| 52642-012-00 | 52642001200 | 200 LOZENGE in 1 BAG (52642-012-00) | 200 lozenge | 2015-04-27 | 0000-00-00 | No | No | Current |