Home NDC 58892-113 TiZO Eye Renewal SPF 20 (Non-Tinted)
Product NDC 58892-113
11-digit product format 588920113
Labeler code 58892
Product ID 58892-113_24c33b97-e472-feca-e063-6394a90ad7d9
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler Fallien Cosmeceuticals, LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-01
Substance ZINC OXIDE
Active strength 90 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 TiZO Eye Renewal SPF 20 (Non-Tinted)
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 90 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 58892-113-15 TiZO Eye Renewal SPF 20 (Non-Tinted) 15 g in 1 BOTTLE, PUMP CREAM 15 3 58892-113-15 TiZO Eye Renewal SPF 20 (Non-Tinted) 1 in 1 CARTON CREAM 1 3 58892-113-05 TiZO Eye Renewal SPF 20 (Non-Tinted) 1.5 g in 1 PACKET CREAM 1.5 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58892-113 TIZO EYE RENEWAL SPF 20 (NON-TINTED) (ZINC OXIDE) CREAM [FALLIEN COSMECEUTICALS, LTD] 3 Current NDC, Legacy NDC, 2 package rows 20241020_33f8760c-2953-44a6-9239-424fdb97a5b3.zip 58892-113 TIZO EYE RENEWAL SPF 20 (NON-TINTED) (ZINC OXIDE) CREAM [FALLIEN COSMECEUTICALS, LTD] 1 Current NDC, Legacy NDC, 1 package rows 20250212_2d40099a-2cfa-1d99-e063-6394a90a36a6.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 Marketing end Sample Exclude flag Status 58892-113-05 58892011305 1.5 g in 1 PACKET (58892-113-05) 1.5 g 2020-09-01 Yes No Current 58892-113-15 58892011315 1 BOTTLE, PUMP in 1 CARTON (58892-113-15) / 15 g in 1 BOTTLE, PUMP 2020-09-01 0000-00-00 No No Current