Ultra Shade Sunscreen SPF 30
- Product NDC
- 70919-001
- 11-digit product format
- 709190001
- Labeler code
- 70919
- Product ID
- 70919-001_98c8ed4d-2427-4e2e-8462-ae2c7ac792fb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- LA LASER CENTE, PC, CALIFORNIA PROFESSIONAL MEDICAL CORP
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-08-17
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 5 g/100mL; g/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70919-001-01 | Ultra Shade Sunscreen SPF 30Taheri MD | 50 mL in 1 BOTTLE, PUMP | CREAM | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70919-001 | ULTRA SHADE SUNSCREEN SPF 30 TAHERI MD (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [LA LASER CENTE, PC, CALIFORNIA PROFESSIONAL MEDICAL CORP] | 2 | Legacy NDC, 1 package rows | 20170106_1d9a237d-5d3a-4ad8-8e58-280a0771bd5f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70919-001-01 | 70919000101 | 50 mL in 1 BOTTLE, PUMP | 50 ml | Historical |