Home NDC 68062-8313 Dr Lift SPF 50 Clear Stick
Product NDC 68062-8313
11-digit product format 680628313
Labeler code 68062
Product ID 68062-8313_40c11b19-fc90-2033-e063-6394a90a5a5f
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form STICK
Route TOPICAL
Labeler Spa de Soleil
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-09
Substance OCTISALATE; OCTOCRYLENE; AVOBENZONE; HOMOSALATE
Active strength .74; 1.48; .4; 1.48 mg/14.8mL; mg/14.8mL; mg/14.8mL; mg/14.8mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Dr Lift SPF 50 Clear Stick
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE .74 mg/14.8mL OCTOCRYLENE 1.48 mg/14.8mL AVOBENZONE .4 mg/14.8mL HOMOSALATE 1.48 mg/14.8mL
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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68062-8313-1 Dr Lift SPF 50 Clear Stick 14.8 mL in 1 TUBE STICK 14.8 1
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 68062-8313-1 68062831301 14.8 mL in 1 TUBE (68062-8313-1) 14.8 ml 2025-10-09 No No Current