Salicylic Acid
- Product NDC
- 37808-523
- 11-digit product format
- 378080523
- Labeler code
- 37808
- Product ID
- 37808-523_c7928047-f060-4582-e053-2995a90ae27f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Medicated Callus Removers
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- HEB
- Application
- part358F
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-12-22
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 40 mg/41
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-523 | SALICYLIC ACID (MEDICATED CALLUS REMOVERS) PATCH [HEB] | 7 | Legacy NDC | 20241212_05e7e7db-4ec0-4cee-b709-d297080b8c7c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37808-523-04 | 37808052304 | 4 PATCH in 1 PACKAGE (37808-523-04) | 4 patch | 2017-12-22 | 0000-00-00 | No | No | Current |