terrasil Foreskin Relief
- Product NDC
- 24909-058
- 11-digit product format
- 249090058
- Labeler code
- 24909
- Product ID
- 24909-058_5c42f560-69ac-83a6-e063-6394a90a1f75
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-01
- Substance
- ALLANTOIN
- Active strength
- .5 g/100g
- 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
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALLANTOIN | .5 g/100g |
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 |
|---|---|---|---|---|---|---|---|
| 24909-058-50 | 24909005850 | 50 g in 1 TUBE (24909-058-50) | 50 g | 2026-10-01 | No | No | Current |
| 24909-058-57 | 24909005857 | 57 g in 1 TUBE (24909-058-57) | 57 g | 2026-10-01 | No | No | Current |