Home NDC 30807-1060 ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN
Product NDC 30807-1060
11-digit product format 308071060
Labeler code 30807
Product ID 30807-1060_47b74894-0916-f792-e063-6394a90aeb22
Type HUMAN OTC DRUG
Nonproprietary name SPF50
Dosage form CREAM
Route TOPICAL
Labeler Wild Child Laboratories PTY Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-12-01
Substance ZINC OXIDE
Active strength 22.75 g/100mL
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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 22.75 g/100mL
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 30807-1060-1 ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN 15 mL in 1 TUBE CREAM 15 5 30807-1060-2 ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN 50 mL in 1 TUBE CREAM 50 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30807-1060 ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN (SPF50) CREAM [WILD CHILD LABORATORIES PTY LTD] 2 Current NDC, 2 package rows 20250227_2767ba3e-7434-d474-e063-6294a90aa4ff.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 30807-1060-1 30807106001 15 mL in 1 TUBE (30807-1060-1) 15 ml 2024-12-01 No No Current 30807-1060-2 30807106002 50 mL in 1 TUBE (30807-1060-2) 50 ml 2024-12-01 No No Current