Regemarine
- Product NDC
- 42248-107
- 11-digit product format
- 422480107
- Labeler code
- 42248
- Product ID
- 42248-107_76b70628-b13f-4273-ac4b-c773c289d8ca
- 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
- 4 mL/50mL
- 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 |
|---|
| 42248-107-02 | RegemarineExtreme | 1 in 1 BOX | CREAM | 1 | | 4 |
| 42248-107-02 | RegemarineExtreme | 50 mL in 1 JAR | CREAM | 50 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42248-107 | REGEMARINE EXTREME (OCTINOXATE) CREAM [ZENITH MEDICOSM SL] | 4 | Legacy NDC, 2 package rows | 20120123_1d93e4ff-471d-44e8-bffa-ff631cde3ca6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42248-107-02 | 42248010702 | 1 in 1 BOX | Historical |