Home NDC 87565-0001-1 Krx Aesthetics All Day Glow Sunblocker
Product NDC 87565-0001
Requested package NDC 87565-0001-1
11-digit product format 875650001
Labeler code 87565
Product ID 87565-0001_4e69c382-9d53-7658-e063-6294a90aefd2
Type HUMAN OTC DRUG
Nonproprietary name Krx Aesthetics All Day Glow Sunblocker
Dosage form CREAM
Route TOPICAL
Labeler BY KIN AESTHETICS LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2024-09-01
Substance OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength 1; 1; 2.5 g/50g; g/50g; g/50g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Krx Aesthetics All Day Glow Sunblocker
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 1 g/50g ZINC OXIDE 1 g/50g TITANIUM DIOXIDE 2.5 g/50g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5A68WGF6WM Internal UNII lookup SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
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 87565-0001-1 Krx Aesthetics All Day Glow Sunblocker 50 g in 1 PACKAGE CREAM 50 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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87565-0001-1 87565000101 50 g in 1 PACKAGE (87565-0001-1) 50 g 2024-09-01 No No Current