Home NDC 53208-003 ISA KNOX UV SUN PRO 365 Sheer Mineral Face
Product NDC 53208-003
11-digit product format 532080003
Labeler code 53208
Product ID 53208-003_32457b13-65e4-94bb-e063-6394a90a955e
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide
Dosage form CREAM
Route TOPICAL
Labeler LG HOUSEHOLD & HEALTH CARE LTD.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-10
Substance ZINC OXIDE
Active strength 155.2 mg/mL
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 ISA KNOX UV SUN PRO 365 Sheer Mineral Face
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 155.2 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 53208-003-01 ISA KNOX UV SUN PRO 365 Sheer Mineral Face 50 mL in 1 BOTTLE CREAM 50 2 53208-003-02 ISA KNOX UV SUN PRO 365 Sheer Mineral Face 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53208-003 ISA KNOX UV SUN PRO 365 SHEER MINERAL FACE (ZINC OXIDE) CREAM [LG HOUSEHOLD & HEALTH CARE LTD.] 2 Current NDC, 2 package rows 20250511_2eeac795-b74e-b3a3-e063-6294a90abf52.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 45 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 53208-003-01 53208000301 50 mL in 1 BOTTLE 50 ml Historical 53208-003-02 53208000302 1 BOTTLE in 1 CARTON (53208-003-02) / 50 mL in 1 BOTTLE (53208-003-01) 1 bottle 2025-05-10 No No Current