Home NDC 70581-019 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
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
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