Home NDC 85241-061 Timesavvy Hybrid XL Cushion Sun Serum SPF 50
Product NDC 85241-061
11-digit product format 852410061
Labeler code 85241
Product ID 85241-061_5328761e-59d2-ca7a-e063-6394a90ae810
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler ProBetter USA, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-01
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength 100; 30; 20; 138.5 mg/g; mg/g; mg/g; mg/g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Timesavvy Hybrid XL Cushion Sun Serum SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/g OCTISALATE 30 mg/g OCTOCRYLENE 20 mg/g ZINC OXIDE 138.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85241-061-00 85241006100 2 CASE in 1 CARTON (85241-061-00) / 25 g in 1 CASE 2 case 2026-05-01 No No Current