Salicylic Acid
- Product NDC
- 69842-294
- Requested package NDC
- 69842-294-09
- 11-digit product format
- 698420294
- Labeler code
- 69842
- Product ID
- 69842-294_c7434f24-3518-a210-e053-2995a90aeefe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrogel Clear Wart Remover
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- CVS Pharmacy
- Application
- part358F
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-02-01
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 40 mg/121
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 | 69842-294 | 69842-294-09 | 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 |
|---|---|---|---|---|---|---|---|---|
| 69842-294-09 | 69842029409 | 12 PATCH in 1 PACKAGE (69842-294-09) | 12 patch | 2020-02-01 | 0000-00-00 | No | No | Current |