Home NDC 85037-002 Sungboon Editor Daily Invisible Blurring Sunscreen
Product NDC 85037-002
11-digit product format 850370002
Labeler code 85037
Product ID 85037-002_534d5429-71a5-7fbf-e063-6394a90a0a39
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler Olive International Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-25
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 29; 100; 49; 90 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 Sungboon Editor Daily Invisible Blurring Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 29 mg/mL HOMOSALATE 100 mg/mL OCTISALATE 49 mg/mL OCTOCRYLENE 90 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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85037-002-01 Sungboon Editor Daily Invisible Blurring Sunscreen 50 mL in 1 TUBE CREAM 50 3 85037-002-02 Sungboon Editor Daily Invisible Blurring Sunscreen 1 in 1 CARTON CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85037-002 SUNGBOON EDITOR DAILY INVISIBLE BLURRING SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) CREAM [OLIVE INTERNATIONAL INC.] 2 Current NDC, 2 package rows 20250327_42325963-0917-43c4-8fe0-130336c7fa81.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 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85037-002-01 85037000201 50 mL in 1 TUBE 50 ml Historical 85037-002-02 85037000202 1 TUBE in 1 CARTON (85037-002-02) / 50 mL in 1 TUBE (85037-002-01) 1 tube 2025-03-25 No No Current 85037-002-04 85037000204 1 TUBE in 1 CARTON (85037-002-04) / 12 mL in 1 TUBE (85037-002-03) 1 tube 2025-06-02 No No Current