FDA.reportPublic FDA data

SHISEIDO ULTIMATE SUN PROTECTOR

Product NDC
58411-480
11-digit product format
584110480
Labeler code
58411
Product ID
58411-480_47a95b3e-c698-9007-e063-6394a90afe66
Type
HUMAN OTC DRUG
Nonproprietary name
OCTISALATE, TITANIUM DIOXIDE, OCTOCRYLENE, and ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
SHISEIDO AMERICAS CORPORATION
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-01
Substance
OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
3.105; 4.347; 2.359; 12.047 g/50mL; g/50mL; g/50mL; g/50mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SHISEIDO ULTIMATE SUN PROTECTOR
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTISALATE3.105 g/50mL
OCTOCRYLENE4.347 g/50mL
TITANIUM DIOXIDE2.359 g/50mL
ZINC OXIDE12.047 g/50mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4X49Y0596W, 5A68WGF6WM, 15FIX9V2JP, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58411-480-60SHISEIDO ULTIMATE SUN PROTECTOR1 in 1 CARTONCREAM13
58411-480-60SHISEIDO ULTIMATE SUN PROTECTOR50 mL in 1 TUBECREAM503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58411-480SHISEIDO ULTIMATE SUN PROTECTOR (OCTISALATE, TITANIUM DIOXIDE, OCTOCRYLENE, AND ZINC OXIDE) CREAM [SHISEIDO AMERICAS CORPORATION]2Current NDC, Legacy NDC, 2 package rows20241225_c656792a-e1ed-478d-b501-9bdc92d16eca.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58411-480-60584110480601 TUBE in 1 CARTON (58411-480-60) / 50 mL in 1 TUBE1 tube2020-01-010000-00-00NoNoCurrent