Menstrual Relief
- Product NDC
- 11673-967
- 11-digit product format
- 116730967
- Labeler code
- 11673
- Product ID
- 11673-967_82a07d3e-0028-484c-8e73-d7cfe0e6811d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen, pamabrom, pyrilamine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-01-13
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; PAMABROM; PYRILAMINE MALEATE
- Active strength
- 500 mg/1; mg/1; 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 | 11673-967 | D | Discontinued by firm | 2026-10-05 | ||
| excluded package | package | 11673-967 | 11673-967-10 | 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 11673-967-10 | 11673096710 | 1 BOTTLE, PLASTIC in 1 CARTON (11673-967-10) > 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2015-01-13 | 0000-00-00 | No | No | Current |