Home NDC 68577-153 KOPARI Sun Shield Soft Glow Daily Face SPF30
Product NDC 68577-153
11-digit product format 685770153
Labeler code 68577
Product ID 68577-153_2a269ead-815c-9047-e063-6294a90ad224
Type HUMAN OTC DRUG
Nonproprietary name Octisalate, Octocrylene, Avobenzone, Homosalate
Dosage form SPRAY
Route TOPICAL
Labeler COSMAX USA, CORPORATION
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-06-01
Substance AVOBENZONE; HOMOSALATE; OCTOCRYLENE; OCTISALATE
Active strength 3; 10; 4; 5 mg/100mg; mg/100mg; mg/100mg; mg/100mg
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 KOPARI Sun Shield Soft Glow Daily Face SPF30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 3 mg/100mg HOMOSALATE 10 mg/100mg OCTOCRYLENE 4 mg/100mg OCTISALATE 5 mg/100mg
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 68577-153-01 KOPARI Sun Shield Soft Glow Daily Face SPF30 100 mg in 1 BOTTLE, SPRAY SPRAY 100 2 68577-153-01 KOPARI Sun Shield Soft Glow Daily Face SPF30 1 in 1 CARTON SPRAY 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68577-153 KOPARI SUN SHIELD SOFT GLOW DAILY FACE SPF30 (OCTISALATE, OCTOCRYLENE, AVOBENZONE, HOMOSALATE) SPRAY [COSMAX USA, CORPORATION] 2 Current NDC, 2 package rows 20241228_0d3673da-822b-09e2-e063-6394a90a348e.zip
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 Marketing start Sample Exclude flag Status 68577-153-01 68577015301 1 BOTTLE, SPRAY in 1 CARTON (68577-153-01) / 100 mg in 1 BOTTLE, SPRAY 2023-06-01 No No Current