Uterus Pentas
- Product NDC
- 53645-2550
- Requested package NDC
- 53645-2550-6
- 11-digit product format
- 536452550
- Labeler code
- 53645
- Product ID
- 53645-2550_548c030c-8bd4-cc84-e063-6294a90a62c9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Uterus Pentas 7X, 11X, 18X, 30X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2026-06-18
- Substance
- BOS TAURUS UTERUS
- Active strength
- 7 [hp_X]/30mL
- 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
- Uterus Pentas
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BOS TAURUS UTERUS | 7 [hp_X]/30mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9169LW451G | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 548bf27d-6b32-81d0-e063-6394a90a1e35 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Uterus Pentas | UTERUS PENTAS 7X, 11X, 18X, 30X | True Botanica, LLC | 548bf27d-6b32-81d0-e063-6394a90a1e35 | 2026-06-18 | Warnings | 53645-2550-6 53645-2550 53645255006 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 53645-2550-6 | 53645255006 | 30 mL in 1 BOTTLE (53645-2550-6) | 30 ml | 2026-06-18 | No | No | Current |