Regemarine
- Product NDC
- 42248-112
- 11-digit product format
- 422480112
- Labeler code
- 42248
- Product ID
- 42248-112_2271626b-8be0-483f-a6a3-5b9f5176f40b
- 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 |
|---|
| 42248-112-01 | RegemarineExtreme | 200 mL in 1 TUBE | CREAM | 200 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42248-112 | REGEMARINE EXTREME (OCTINOXATE) CREAM [ZENITH MEDICOSM SL] | 4 | Legacy NDC, 1 package rows | 20120123_b861c8ea-3206-4bf4-b210-7d1ee442456c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 42248-112-01 | 42248011201 | 200 mL in 1 TUBE | 200 ml | Historical |