MDSolarSciences SPF50 Plus Ultra Mineral Screen

Product NDC
17452-380
11-digit product format
174520380
Labeler code
17452
Product ID
17452-380_f1e2b580-adac-4eb6-b736-0cfb31f8326b
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide and Zinc Oxide
Dosage form
GEL
Route
TOPICAL
Labeler
Ecometics, Inc
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2010-03-01
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
10 g/100g; g/100g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17452-380-012019-10-29C16284748780-1960f7f55-c40d-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17452-380-01MDSolarSciences SPF50 Plus Ultra Mineral Screen50 g in 1 TUBEGEL502

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17452-380MDSOLARSCIENCES SPF50 PLUS ULTRA MINERAL SCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) GEL [ECOMETICS, INC]2Legacy NDC, 1 package rows20101116_e5d3dd27-6b10-4b01-b422-af880783cbf0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
17452-380-011745203800150 g in 1 TUBE50 gHistorical