NDC 58443-0621 - Frida Mom Healing Foam
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 58443-0621
- Package NDCs from labels
- 58443-0621-4
- Manufacturer
- Prime Enterprises, Inc.
- Effective date
- 2023-05-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Frida mom Perineal Healing Foam | Prime Enterprises, Inc. | 2023-05-23 | HUMAN OTC DRUG LABEL |
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.
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| Hand Sanitizer | ALCOHOL | Trifecta Pharmaceuticals USA | 0ba469a8-53f3-eb8e-e063-6294a90a1efc | 2026-03-04 | Warnings | 3K9958V90M |
| Avant Foaming Hand Sanitizer | ALCOHOL | B4 Soap LLC | 6cc57ff1-e49b-4c15-b997-886a29d3fe1c | 2026-03-04 | Warnings | 3K9958V90M |
| Smart Care FRENCH VANILLA HAND SANITIZER | ETHYL ALCOHOL | Ashtel Studios Inc. | 047f107b-c4d7-42d4-9c9c-5af8280be758 | 2026-03-04 | Warnings | 3K9958V90M |
| Everyone Hand Sanitizer Lavender Aloe | ALCOHOL | EO Products, LLC | d15c1fb9-b25b-45b8-a119-ee4c86c8d91c | 2026-03-03 | Warnings | 3K9958V90M |
| Advanced Hand Sanitizer | ETHYL ALCOHOL | Amazon.Com Services LLC | 85421e9a-f1c9-4793-9479-8a072a610ed7 | 2026-03-03 | Warnings, Adverse reactions | 3K9958V90M |
| Witch Hazel | WITCH HAZEL | Amazon.com Services LLC | 134e07a1-5236-4088-baf9-1ff33126f793 | 2026-03-03 | Warnings, Adverse reactions | 101I4J0U34 |
| FOOTSPA PEDI | ALCOHOL | CHEMCO CORPORATION | 3886a958-d035-ed15-e063-6294a90af1b5 | 2026-03-03 | Warnings | 3K9958V90M |
| Anti Bacterial Moisturizing Hand Sanitizer Starfruit Sangria | ALCOHOL | Bath & Body Works, Inc. | 387caf6b-fda0-a63f-e063-6294a90a041a | 2026-03-03 | Warnings | 3K9958V90M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.