Home NDC 59062-1000 SPF 50 plus Sunscreen
Product NDC 59062-1000
11-digit product format 590621000
Labeler code 59062
Product ID 59062-1000_a7636b53-d9d4-4c4f-929a-515a8cc78659
Type HUMAN OTC DRUG
Nonproprietary name Titanium Dioxide, OCTISALATE, and ZINC OXIDE
Dosage form LOTION
Route TOPICAL
Labeler KAS Direct LLC dba BabyGanics
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-07-24
Marketing end 2026-12-31
Substance TITANIUM DIOXIDE; OCTISALATE; ZINC OXIDE
Active strength 30; 50; 60 mg/mL; mg/mL; mg/mL
NDC exclude flag No
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 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 30 mg/mL OCTISALATE 50 mg/mL ZINC OXIDE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup 4X49Y0596W Internal UNII lookup 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 59062-1000-1 SPF 50 plus Sunscreen 354 mL in 1 TUBE LOTION 354 2 59062-1000-2 SPF 50 plus Sunscreen 59 mL in 1 TUBE LOTION 59 2 59062-1000-2 outdoor explorer set 59 mL in 1 TUBE LOTION 59 mL 50 mg in 1mL 2 59062-1000-6 SPF 50 plus Sunscreen 177 mL in 1 TUBE LOTION 177 2 59062-1000-8 SPF 50 plus Sunscreen 236 mL in 1 TUBE LOTION 236 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59062-1000 OUTDOOR EXPLORER SET (TITANIUM DIOXIDE, OCTISALATE, AND ZINC OXIDE) KIT [KAS DIRECT LLC DBA BABYGANICS] 2 Current NDC, Legacy NDC 20210720_726096c2-514a-439a-9697-346ca684c493.zip 59062-1000 SPF 50 PLUS SUNSCREEN (TITANIUM DIOXIDE, OCTISALATE, AND ZINC OXIDE) LOTION [KAS DIRECT LLC DBA BABYGANICS] 2 Current NDC, Legacy NDC, 4 package rows 20241220_5a4c71fc-aa6f-47f7-8d1d-2af2e726cf9b.zip 59062-1000 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 162 of 353 · 7,041 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 59062-1000-1 59062100001 354 mL in 1 TUBE (59062-1000-1) 354 ml 2017-07-24 0000-00-00 No No Current 59062-1000-2 59062100002 59 mL in 1 TUBE (59062-1000-2) 59 ml 2017-07-24 0000-00-00 No No Current 59062-1000-6 59062100006 177 mL in 1 TUBE (59062-1000-6) 177 ml 2017-07-24 0000-00-00 No No Current 59062-1000-8 59062100008 236 mL in 1 TUBE (59062-1000-8) 236 ml 2017-07-24 2026-12-31 No No Current