Salicylic acid
- Product NDC
- 68016-230
- 11-digit product format
- 680160230
- Labeler code
- 68016
- Product ID
- 68016-230_489e1114-2f04-4f8d-b4d1-7b25022a587e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Medicated Callus Removers Extra Thick
- Dosage form
- PATCH
- Route
- TOPICAL
- Labeler
- Chain Drug Consortium, LLC
- Application
- part358F
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-02-12
- Marketing end
- 0000-00-00
- Substance
- SALICYLIC ACID
- Active strength
- 40 mg/41
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68016-230-04 | Salicylic acid | 4 in 1 PACKAGE | PATCH | 4 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68016-230 | SALICYLIC ACID (MEDICATED CALLUS REMOVERS EXTRA THICK) PATCH [CHAIN DRUG CONSORTIUM, LLC] | 2 | Legacy NDC, 1 package rows | 20191213_f9939024-fdcb-42bd-9f25-b5bafa79a876.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68016-230-04 | 68016023004 | 4 PATCH in 1 PACKAGE (68016-230-04) | 4 patch | 2018-02-12 | 0000-00-00 | No | No | Current |