FDA.reportPublic FDA data

Sun Bum Face 50 Premium Sunscreen SPF 50

Product NDC
44717-080
11-digit product format
447170080
Labeler code
44717
Product ID
44717-080_40d36900-8fdd-17ae-e063-6394a90ab565
Type
HUMAN OTC DRUG
Nonproprietary name
Avobenzone, Homosalte, Octisalate, Octocrylene
Dosage form
LOTION
Route
TOPICAL
Labeler
Wasatch Product Development, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-02-01
Substance
AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength
3; 10; 5; 10 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sun Bum Face 50 Premium Sunscreen SPF 50
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AVOBENZONE3 g/100mL
HOMOSALATE10 g/100mL
OCTISALATE5 g/100mL
OCTOCRYLENE10 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiG63QQF2NOX, V06SV4M95S, 4X49Y0596W, 5A68WGF6WM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44717-080-01Sun Bum Face 50 Premium Sunscreen SPF 5088 mL in 1 TUBELOTION883

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44717-080SUN BUM FACE 50 PREMIUM SUNSCREEN SPF 50 (AVOBENZONE, HOMOSALTE, OCTISALATE, OCTOCRYLENE) LOTION [WASATCH PRODUCT DEVELOPMENT, LLC]2Current NDC, 1 package rows20241024_f4ac746a-a50a-8041-e053-2a95a90a8ea6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
44717-080-014471700800188 mL in 1 TUBE (44717-080-01) 88 ml2023-02-01NoNoCurrent