Salicylic Acid
- Product NDC
- 68016-607
- 11-digit product format
- 680160607
- Labeler code
- 68016
- Product ID
- 68016-607_c78db256-d888-ed58-e053-2995a90ae658
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Medicated Callus Removers
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- part358F
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2003-05-23
- 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 Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68016-607 | SALICYLIC ACID (MEDICATED CALLUS REMOVERS) PATCH [CHAIN DRUG CONSORTIUM, LLC] | 10 | Legacy NDC | 20241213_b4dea916-f4e9-4531-a539-d069f893953d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68016-607-00 | 68016060700 | 4 PATCH in 1 PACKAGE (68016-607-00) | 4 patch | 2003-05-23 | 0000-00-00 | No | No | Current |