TERAPIA DE DIA Y NOCHE
- Product NDC
- 87943-085
- 11-digit product format
- 879430085
- Labeler code
- 87943
- Product ID
- 87943-085_59f44135-865c-9d7d-e063-6294a90a9dd9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pain Relieving Patch
- Dosage form
- KIT
- Route
- TOPICAL
- Labeler
- DW SUPPORT LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-20
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TERAPIA DE DIA Y NOCHE
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 59f44135-865b-9d7d-e063-6294a90a9dd9 | Available on FDA.report |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 87943-085-20 | 87943008520 | 1 KIT in 1 KIT (87943-085-20) * 12 g in 1 PATCH (87943-012-01) * 12 g in 1 PATCH (87943-016-01) | 1 kit | 2026-08-20 | No | No | Current |