Home NDC 10596-804 Hello Sunday The Mineral One Lightweight Serum SPF 50
Product NDC 10596-804
11-digit product format 105960804
Labeler code 10596
Product ID 10596-804_2d083748-82aa-f046-e063-6294a90aea80
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form EMULSION
Route TOPICAL
Labeler Kao USA Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-02-01
Substance ZINC OXIDE
Active strength 175.2 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 10596-804-01 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 10596-804-01 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 10596-804-01 0efc9e666f02…f202fb6c5f17…
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 Hello Sunday The Mineral One Lightweight Serum SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 175.2 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10596-804-01 Hello Sunday The Mineral One Lightweight Serum SPF 50 1 in 1 CARTON EMULSION 1 2 10596-804-01 Hello Sunday The Mineral One Lightweight Serum SPF 50 30 mL in 1 BOTTLE EMULSION 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10596-804 HELLO SUNDAY THE MINERAL ONE LIGHTWEIGHT SERUM SPF 50 (ZINC OXIDE) EMULSION [KAO USA INC.] 2 Current NDC, 2 package rows 20250202_0c91894f-a40e-73e9-e063-6394a90ab807.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 Units Marketing start Sample Exclude flag Status 10596-804-01 10596080401 1 BOTTLE in 1 CARTON (10596-804-01) / 30 mL in 1 BOTTLE 1 bottle 2024-02-01 No No Current