Desert Sun Protection Broad Spectrum SPF 25
- Product NDC
- 82323-2650
- 11-digit product format
- 823232650
- Labeler code
- 82323
- Product ID
- 82323-2650_ea363654-6180-38e9-e053-2995a90ab125
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate and Zinc Oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Boise Image Enhancement Centre PA
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-08-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 7 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82323-2650-2 | Desert Sun Protection Broad Spectrum SPF 25 | 50 mL in 1 BOTTLE, PUMP | LOTION | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82323-2650 | DESERT SUN PROTECTION BROAD SPECTRUM SPF 25 (OCTINOXATE AND ZINC OXIDE) LOTION [BOISE IMAGE ENHANCEMENT CENTRE PA] | 2 | Legacy NDC, 1 package rows | 20240117_ea362e16-e6f0-b7cb-e053-2a95a90abffc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82323-2650-2 | 82323265002 | 50 mL in 1 BOTTLE, PUMP (82323-2650-2) | 50 ml | 2022-08-01 | 0000-00-00 | No | No | Current |