Home DailyMed 1bb4a177-034c-e79d-e063-6294a90ab732 Nubes SUN BLOCK Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer UNIQUEMI | Kolmar Korea Co., Ltd
Effective date 2024-06-25
Label type HUMAN OTC DRUG LABEL
Version 1
Source full-release
Hydrated at 2026-06-01 00:14:37 Label at a glance# Product Nubes SUN BLOCK
Active ingredient HOMOSALATE, OCTINOXATE, OCTISALATE, AVOBENZONE, OCTOCRYLENE
Label structure 8 sections
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84514-0001-1 Nubes SUN BLOCK 52 mL in 1 CONTAINER CREAM 52 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84514-0001 NUBES SUN BLOCK (HOMOSALATE, OCTINOXATE, OCTOCRYLENE,, AVOBENZONE) CREAM [UNIQUEMI] 1 1 package rows 20240704_1bb4a177-034c-e79d-e063-6294a90ab732.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 8 matching rows.
Nubes SUN BLOCK Homosalate, Octinoxate, Octocrylene,, Avobenzone HOMOSALATE WATER OCTINOXATE OCTISALATE AVOBENZONE OCTOCRYLENE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 6 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 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.