CVS Pain Relieving
- Product NDC
- 51316-885
- Requested package NDC
- 51316-885-16
- 11-digit product format
- 513160885
- Labeler code
- 51316
- Product ID
- 51316-885_f0335578-035d-49b4-e053-2a95a90ad65e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor 5.5% Menthol 16%
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- CVS
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-12-19
- Marketing end
- 0000-00-00
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 16 mg/g; mg/g
- 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 | 51316-885 | 51316-885-16 | 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 |
|---|---|---|---|---|---|---|---|---|
| 51316-885-16 | 51316088516 | 72 g in 1 TUBE (51316-885-16) | 72 g | 2022-12-19 | 0000-00-00 | No | No | Current |