Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen

Product NDC
49967-595
11-digit product format
499670595
Labeler code
49967
Product ID
49967-595_676f1412-f75f-4dc4-a76a-57c360aeb54c
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium dioxide
Dosage form
LOTION
Route
TOPICAL
Labeler
L'Oreal USA Products Inc
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2013-06-01
Substance
TITANIUM DIOXIDE
Active strength
110 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TITANIUM DIOXIDE110 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii15FIX9V2JP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49967-595-01Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen150 mL in 1 BOTTLE, PLASTICLOTION1509

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49967-595KIEHLS SINCE 1851 ACTIVATED SUN PROTECTOR FOR FACE AND BODY BROAD SPECTRUM SPF 50 SUNSCREEN (TITANIUM DIOXIDE) LOTION [L'OREAL USA PRODUCTS INC]9Current NDC, Legacy NDC, 1 package rows20241229_87496037-36ca-4c5f-973f-46626cf4096e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49967-595-0149967059501150 mL in 1 BOTTLE, PLASTIC (49967-595-01) 150 ml2013-06-010000-00-00NoNoCurrent