Home NDC 82800-010 Prequel Sun Barrier Mineral Sunscreen Broad Spectrum SPF 50
Product NDC 82800-010
11-digit product format 828000010
Labeler code 82800
Product ID 82800-010_2bf08ea6-beb4-7556-e063-6394a90a01d9
Type HUMAN OTC DRUG
Nonproprietary name Mineral Sunscreen
Dosage form CREAM
Route TOPICAL
Labeler The Center Brands, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-09-21
Substance ZINC OXIDE
Active strength 18 mg/g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Prequel Sun Barrier Mineral Sunscreen Broad Spectrum SPF 50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 18 mg/g
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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82800-010-01 Prequel Sun Barrier Mineral Sunscreen Broad Spectrum SPF 50 50 g in 1 TUBE CREAM 50 3 82800-010-01 Prequel Sun Barrier Mineral Sunscreen Broad Spectrum SPF 50 1 in 1 PACKAGE CREAM 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82800-010 PREQUEL SUN BARRIER MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 (MINERAL SUNSCREEN) CREAM [THE CENTER BRANDS, LLC] 3 Current NDC, 2 package rows 20250119_cd35ae20-d5b7-479d-8a5e-0278eae9e83c.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 82800-010-01 82800001001 1 TUBE in 1 PACKAGE (82800-010-01) / 50 g in 1 TUBE 1 tube 2023-09-21 No No Current