DERMAPROT
- Product NDC
- 66854-013
- 11-digit product format
- 668540013
- Labeler code
- 66854
- Product ID
- 66854-013_02b48851-bdcc-4a02-8168-35a65d768f73
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRICLOSAN
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
- Application
- part333E
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-05-31
- Marketing end
- 0000-00-00
- Substance
- TRICLOSAN
- Active strength
- 0 mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 66854-013-01 | DERMAPROTTRICLOTREX-B | 500 mL in 1 JAR | LIQUID | 500 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66854-013 | DERMAPROT TRICLOTREX-B (TRICLOSAN) LIQUID [SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS] | 1 | Legacy NDC, 1 package rows | 20120531_43311fc9-21c3-45f2-8083-06e3f1742d91.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 66854-013-01 | 66854001301 | 500 mL in 1 JAR | 500 ml | Historical |