Home NDC 84130-017 Sunglaze Body Gel Cream Sunscreen SPF50
Product NDC 84130-017
11-digit product format 841300017
Labeler code 84130
Product ID 84130-017_3e6658a1-ae6b-9d19-e063-6294a90acae7
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octisalate, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler Koco Life LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-09
Substance OCTISALATE; AVOBENZONE; HOMOSALATE; OCTOCRYLENE
Active strength 30; 40; 30; 30 mg/mL; mg/mL; mg/mL; mg/mL
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 Sunglaze Body Gel Cream Sunscreen SPF50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 30 mg/mL AVOBENZONE 40 mg/mL HOMOSALATE 30 mg/mL OCTOCRYLENE 30 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 84130-017-33 Sunglaze Body Gel Cream Sunscreen SPF50 100 mL in 1 TUBE CREAM 100 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 84130-017-33 84130001733 100 mL in 1 TUBE (84130-017-33) 100 ml 2025-09-09 No No Current