Home NDC 69968-1013 Neutrogena Ultra Sheer Daily Face Sunscreen Broad Spectrum SPF 70
Product NDC 69968-1013
11-digit product format 699681013
Labeler code 69968
Product ID 69968-1013_58d3d3a5-d7d1-a651-e063-6394a90aad64
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Bemotrizinol, Homosalate, Octisalate
Dosage form LOTION
Route TOPICAL
Labeler Kenvue Brands LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-13
Substance AVOBENZONE; BEMOTRIZINOL; HOMOSALATE; OCTISALATE
Active strength 30; 60; 150; 50 mg/mL; mg/mL; mg/mL; mg/mL
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 Neutrogena Ultra Sheer Daily Face Sunscreen Broad Spectrum SPF 70
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL BEMOTRIZINOL 60 mg/mL HOMOSALATE 150 mg/mL OCTISALATE 50 mg/mL
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 45 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 69968-1013-1 69968101301 1 BOTTLE in 1 CARTON (69968-1013-1) / 40 mL in 1 BOTTLE 1 bottle 2026-08-13 No No Current 69968-1013-2 69968101302 12 TUBE in 1 TRAY (69968-1013-2) / 14 mL in 1 TUBE 12 tube 2026-08-13 No No Current