Desert Sun Protection Broad Spectrum SPF30

Product NDC
82323-0650
11-digit product format
823230650
Labeler code
82323
Product ID
82323-0650_ea35c6b7-c1d9-bc81-e053-2995a90a0670
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide and Zinc Oxide
Dosage form
CREAM
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
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
8 g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82323-0650-2Desert Sun Protection Broad Spectrum SPF3050 mL in 1 BOTTLECREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82323-0650DESERT SUN PROTECTION BROAD SPECTRUM SPF30 (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [BOISE IMAGE ENHANCEMENT CENTRE PA]2Legacy NDC, 1 package rows20240117_ea36371a-b768-e335-e053-2a95a90a60a7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82323-0650-28232306500250 mL in 1 BOTTLE (82323-0650-2) 50 ml2022-08-010000-00-00NoNoCurrent