10 Armani Prima Control Glow Moisturizer SBS SPF 35
- Product NDC
- 70581-019
- 11-digit product format
- 705810019
- Labeler code
- 70581
- Product ID
- 70581-019_9af0650e-2866-75fc-e053-2a95a90a484b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, TITANIUM DIOXIDE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BPS 60
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 50 mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70581-019-00 | 10 Armani Prima Control Glow Moisturizer SBS SPF 35 | 30 mL in 1 TUBE | CREAM | 30 | | 4 |
| 70581-019-00 | 10 Armani Prima Control Glow Moisturizer SBS SPF 35 | 1 in 1 BOX | CREAM | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70581-019 | 10 ARMANI PRIMA CONTROL GLOW MOISTURIZER SBS SPF 35 (OCTINOXATE, TITANIUM DIOXIDE) CREAM [BPS 60] | 4 | Legacy NDC, 2 package rows | 20231216_9dc66fbf-bc66-4c60-9675-05b193da91da.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70581-019-00 | 70581001900 | 1 TUBE in 1 BOX (70581-019-00) > 30 mL in 1 TUBE | 1 tube | 2018-01-01 | 0000-00-00 | No | No | Current |