PC529 ULTREX
- Product NDC
- 10685-529
- 11-digit product format
- 106850529
- Labeler code
- 10685
- Product ID
- 10685-529_6416fa98-1660-1068-e053-2a91aa0acdca
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CHLOROXYLENOL
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- CARROLL COMPANY
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-01-21
- Marketing end
- 0000-00-00
- Substance
- CHLOROXYLENOL
- Active strength
- 3 g/1000mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 10685-529-17 | PC529 ULTREX | 800 mL in 1 BAG | SOAP | 800 | | 2 |
| 10685-529-28 | PC529 ULTREX | 3785 mL in 1 BOTTLE, PLASTIC | SOAP | 3785 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10685-529 | PC529 ULTREX (CHLOROXYLENOL) SOAP [CARROLL COMPANY] | 2 | Legacy NDC, 2 package rows | 20180201_fbf4cfcd-b826-40c7-a344-b9846a61c8cf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 10685-529-17 | 10685052917 | 800 mL in 1 BAG | 800 ml | Historical |
| 10685-529-28 | 10685052928 | 3785 mL in 1 BOTTLE, PLASTIC | 3785 ml | Historical |