Terrasil Itch, Rash and Pain Relief
- Product NDC
- 24909-159
- Requested package NDC
- 24909-159-14
- 11-digit product format
- 249090159
- Labeler code
- 24909
- Product ID
- 24909-159_89966582-906b-46d0-9c18-3998760de58d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin, Menthol
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Aidance Skincare & Topical Solutions, LLC
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-01-01
- Marketing end
- 0000-00-00
- Substance
- ALLANTOIN; MENTHOL
- Active strength
- 1 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 24909-159 | 24909-159-14 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 24909-159-14 | 24909015914 | 14 g in 1 TUBE (24909-159-14) | 14 g | 2017-01-01 | 0000-00-00 | No | No | Current |