Home NDC 58892-211 Proceuticals Private Label by TiZO non-tinted foaming mineral sunscreen
Product NDC 58892-211
11-digit product format 588920211
Labeler code 58892
Product ID 58892-211_1f44ac28-b032-ccff-e063-6394a90a4198
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, Zinc Oxide
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Fallien Cosmeceuticals, Ltd
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-08-09
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 30; 100 mg/g; mg/g
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 Proceuticals Private Label by TiZO non-tinted foaming mineral sunscreen
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 30 mg/g ZINC OXIDE 100 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup 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 58892-211-01 Proceuticals Private Label by TiZO non-tinted foaming mineral sunscreen 100 g in 1 CAN AEROSOL, FOAM 100 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58892-211 PROCEUTICALS PRIVATE LABEL BY TIZO NON-TINTED FOAMING MINERAL SUNSCREEN (TITANIUM DIOXIDE, ZINC OXIDE) AEROSOL, FOAM [FALLIEN COSMECEUTICALS, LTD] 4 Current NDC, 1 package rows 20240810_1f4491ab-95b0-cc14-e063-6394a90a73ca.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 58892-211-01 58892021101 100 g in 1 CAN (58892-211-01) 100 g 2024-08-09 No No Current