Dermesse Sunscreen SPF30
- Product NDC
- 68723-330
- 11-digit product format
- 687230330
- Labeler code
- 68723
- Product ID
- 68723-330_5adfb392-5731-496b-b352-2434161b7b9b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Titanium Dioxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Axia Medical Solutions, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-04-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 70 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68723-330-02 | Dermesse Sunscreen SPF30 | 57 g in 1 BOTTLE | LOTION | 57 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68723-330 | DERMESSE SUNSCREEN SPF30 (OCTINOXATE, TITANIUM DIOXIDE) LOTION [AXIA MEDICAL SOLUTIONS, LLC] | 4 | Legacy NDC, 1 package rows | 20210713_f948c01f-07c9-4c88-ac4c-cb9e504f14fd.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68723-330-02 | 68723033002 | 57 g in 1 BOTTLE (68723-330-02) | 57 g | 2012-04-01 | 0000-00-00 | No | No | Current |