Home NDC 59062-1200 SPF 50 plus Sunscreen
Product NDC 59062-1200
11-digit product format 590621200
Labeler code 59062
Product ID 59062-1200_d1f4c797-2359-448a-8112-f69f227f475d
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE and ZINC OXIDE
Dosage form STICK
Route TOPICAL
Labeler KAS Direct LLC dba BabyGanics
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-06-21
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 79; 67 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 SPF 50 plus Sunscreen
Brand name suffix All Mineral Active Ingredients
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 79 mg/g ZINC OXIDE 67 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 59062-1200-1 SPF 50 plus Sunscreen All Mineral Active Ingredients 13 g in 1 APPLICATOR STICK 13 3 59062-1200-1 SPF 50 plus Sunscreen All Mineral Active Ingredients 1 in 1 BLISTER PACK STICK 1 3 59062-1200-2 SPF 50 plus Sunscreen All Mineral Active Ingredients 2 in 1 BLISTER PACK STICK 2 3 59062-1200-2 SPF 50 plus Sunscreen All Mineral Active Ingredients 13 g in 1 APPLICATOR STICK 13 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59062-1200 SPF 50 PLUS SUNSCREEN ALL MINERAL ACTIVE INGREDIENTS (TITANIUM DIOXIDE AND ZINC OXIDE) STICK KIDS SPF 50 PLUS SUNSCREEN ALL MINERAL ACTIVE INGREDIENTS (TITANIUM DIOXIDE AND ZINC OXIDE) STICK [KAS DIRECT LLC DBA BABYGANICS] 3 Current NDC, Legacy NDC, 4 package rows 20241222_247aae3d-1845-4dd8-b774-b9e8214809a2.zip 59062-1200 SUNCARE ESSENTIALS (TITANIUM DIOXIDE, OCTISALATE, AND ZINC OXIDE) KIT [KAS DIRECT LLC DBA BABYGANICS] 2 Current NDC, Legacy NDC 20250104_96fd2cf8-cb07-4ec1-8946-8e862f6d8377.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 59062-1200-1 59062120001 1 APPLICATOR in 1 BLISTER PACK (59062-1200-1) / 13 g in 1 APPLICATOR 1 applicator 2013-06-21 0000-00-00 No No Current 59062-1200-2 59062120002 2 APPLICATOR in 1 BLISTER PACK (59062-1200-2) / 13 g in 1 APPLICATOR 2 applicator 2013-06-21 0000-00-00 No No Current