terrasil Foreskin Relief Kit
- Product NDC
- 24909-068
- 11-digit product format
- 249090068
- Labeler code
- 24909
- Product ID
- 24909-068_5c43ff95-8a13-1cc6-e063-6294a90af2bd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- KIT
- Route
- TOPICAL
- Labeler
- Aidance Scientific, Inc., DBA Aidance Skincare & Topical Solutions
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-01
- 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
- terrasil Foreskin Relief Kit
- Listing expiration
- 2027-12-31
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 |
|---|---|---|---|---|---|---|---|
| 24909-068-01 | 24909006801 | 1 KIT in 1 KIT (24909-068-01) * 85 g in 1 BOX * 57 g in 1 TUBE (24909-058-57) | 1 kit | 2026-10-01 | No | No | Current |