Elevated Ultimate Tinted Sun Defense Broad Spectrum SPF 30 (UVA/UVB) Sunscreen
- Product NDC
- 81688-0650
- 11-digit product format
- 816880650
- Labeler code
- 81688
- Product ID
- 81688-0650_c16e2c15-0645-4c41-e053-2995a90a4324
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide and Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Elevated Dermatology and Skin
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-02-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 8 g/100mL; g/100mL
- 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 |
|---|
| 81688-0650-3 | Elevated Ultimate Tinted Sun Defense Broad Spectrum SPF 30 (UVA/UVB) Sunscreen | 50 mL in 1 BOTTLE, PUMP | CREAM | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81688-0650 | ELEVATED ULTIMATE TINTED SUN DEFENSE BROAD SPECTRUM SPF 30 (UVA/UVB) SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [ELEVATED DERMATOLOGY AND SKIN] | 1 | Legacy NDC, 1 package rows | 20210504_c16e2c01-6167-9fff-e053-2995a90a2c40.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81688-0650-3 | 81688065003 | 50 mL in 1 BOTTLE, PUMP (81688-0650-3) | 50 ml | 2021-02-01 | 0000-00-00 | No | No | Current |