Hydromarine
- Product NDC
- 42248-110
- 11-digit product format
- 422480110
- Labeler code
- 42248
- Product ID
- 42248-110_fba51ef7-8b81-4b54-9707-b2c75667b4a5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Zenith Medicosm SL
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2011-08-15
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE
- Active strength
- 15 mL/200mL
- 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 |
|---|
| 42248-110-01 | HydromarineExtreme | 200 mL in 1 TUBE | CREAM | 200 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42248-110 | HYDROMARINE EXTREME (OCTINOXATE) CREAM [ZENITH MEDICOSM SL] | 5 | Legacy NDC, 1 package rows | 20120123_08aa016c-53af-47dc-9dd7-c497ea62b587.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 42248-110-01 | 42248011001 | 200 mL in 1 TUBE | 200 ml | Historical |