NDC 24909-189 - Terrasil Rapid-Relief Vaginal
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
- 24909-189
- Package NDCs from labels
- 24909-189-25
- Manufacturer
- Aidance Skincare & Topical Solutions, LLC
- Effective date
- 2018-12-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Terrasil Rapid-Relief Vaginal - Aidance Skincare & Topical Solutions, LLC | Aidance Skincare & Topical Solutions, LLC | 2018-12-29 | 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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| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | B. Braun Medical Inc. | f6d82772-638c-4584-b9d3-8833669f5963 | 2025-11-05 | Warnings, Adverse reactions | 451W47IQ8X |
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| Vertra Ehukai Beige Face Stick SPF 38 | TITANIUM DIOXIDE | Toshiki Pigment Co., ltd. | b71619c4-a8ef-1dda-e053-2995a90aba50 | 2025-11-04 | Warnings | 15FIX9V2JP |
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| Land Shark Zinky SPF 36 Azure Blue | ZINC OXIDE | Tropical Seas, Inc. | d23fe61a-3ffb-59d0-e053-2995a90a59e6 | 2025-11-04 | Warnings | SOI2LOH54Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.