Home NDC 62839-2652 Sunright Solar Screen Mineral Face Sunscreen
Product NDC 62839-2652
11-digit product format 628392652
Labeler code 62839
Product ID 62839-2652_7d542e2d-d92f-460a-b751-ffed79064712
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler NSE Products, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-01
Substance ZINC OXIDE
Active strength 180 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 Sunright Solar Screen Mineral Face Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 180 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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62839-2652-1 Sunright Solar Screen Mineral Face Sunscreen 1 in 1 CARTON LOTION 1 1 62839-2652-1 Sunright Solar Screen Mineral Face Sunscreen 50 mL in 1 TUBE LOTION 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 81 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 62839-2652-1 62839265201 1 TUBE in 1 CARTON (62839-2652-1) / 50 mL in 1 TUBE 1 tube 2024-05-01 No No Current