Sun Bum Face Cream 50 Premium Sunscreen

Product NDC
69039-799
11-digit product format
690390799
Labeler code
69039
Product ID
69039-799_3c57fcf7-7817-8197-e063-6394a90af80a
Type
HUMAN OTC DRUG
Nonproprietary name
HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
Sun Bum, LLC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-01
Substance
HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
100; 50; 100; 70 mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
V06SV4M95SHOMOSALATE118-56-9HOMOSALATE
4X49Y0596WOCTISALATE118-60-5OCTISALATE
5A68WGF6WMOCTOCRYLENE6197-30-4OCTOCRYLENE
SOI2LOH54ZZINC OXIDE1314-13-2ZINC OXIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69039-799-02690390799021 CONTAINER in 1 BOX (69039-799-02) / 30 mL in 1 CONTAINER (69039-799-01) 1 container2025-01-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sun Bum Face Cream 50 Premium SunscreenSun Bum, LLC2025-08-14HUMAN OTC DRUG LABEL1