Home NDC 84803-115 Ultra Violette Velvet Screen Blurring Mineral Skinscreen Broad Spectrum SPF 40
Product NDC 84803-115
11-digit product format 848030115
Labeler code 84803
Product ID 84803-115_5474d16b-49f3-00f9-e063-6394a90aca99
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler Grace and Fire USA Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-27
Substance ZINC OXIDE
Active strength 250 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 Ultra Violette Velvet Screen Blurring Mineral Skinscreen Broad Spectrum SPF 40
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 250 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# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84803-115-50 Ultra Violette Velvet Screen Blurring Mineral Skinscreen Broad Spectrum SPF 40 50 mL in 1 TUBE 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 81 of 354 · 7,077 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84803-115-50 84803011550 50 mL in 1 TUBE (84803-115-50) 50 ml 2026-05-27 No No Current