GREEN FARM POTENT COOLING RELIEF
- Product NDC
- 72937-026
- 11-digit product format
- 729370026
- Labeler code
- 72937
- Product ID
- 72937-026_ef167336-8a71-eca1-e053-2995a90aeeee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, CAMPHOR
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SUNSET NOVELTIES, INC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-12-05
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 2 g/100mL; g/100mL
- 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 | 72937-026 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 72937-026 | 72937-026-02 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 72937-026 | 72937-026-04 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 72937-026 | 72937-026-08 | D | Discontinued by firm | 2026-10-05 | |
| excluded package | package | 72937-026 | 72937-026-16 | D | Discontinued by firm | 2026-10-05 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Dataset | Scope | Package NDC |
|---|---|---|
| excluded product | product | |
| excluded package | package | 72937-026-04 |
| excluded package | package | 72937-026-08 |
| excluded package | package | 72937-026-16 |
| excluded package | package | 72937-026-02 |
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 |
|---|---|---|---|---|---|---|---|---|
| 72937-026-02 | 72937002602 | 60 mL in 1 BOTTLE (72937-026-02) | 60 ml | 2022-12-05 | 0000-00-00 | No | No | Current |
| 72937-026-04 | 72937002604 | 118 mL in 1 BOTTLE (72937-026-04) | 118 ml | 2022-12-05 | 0000-00-00 | No | No | Current |
| 72937-026-08 | 72937002608 | 237 mL in 1 BOTTLE (72937-026-08) | 237 ml | 2022-12-05 | 0000-00-00 | No | No | Current |
| 72937-026-16 | 72937002616 | 473 mL in 1 BOTTLE (72937-026-16) | 473 ml | 2022-12-05 | 0000-00-00 | No | No | Current |