Home NDC 59062-2200 Kids SPF 50 plus Sunscreen
Product NDC 59062-2200
11-digit product format 590622200
Labeler code 59062
Product ID 59062-2200_1b144c6f-8c4c-45bd-ac9f-665b4119f156
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE and ZINC OXIDE
Dosage form STICK
Route TOPICAL
Labeler KAS Direct LLC dba BabyGanics
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2013-06-21
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 79 mg/g; mg/g
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59062-2200-4 Kids SPF 50 plus Sunscreen All Mineral Active Ingredients 45.5 g in 1 APPLICATOR STICK 45.5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59062-2200 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 Legacy NDC, 1 package rows 20241222_247aae3d-1845-4dd8-b774-b9e8214809a2.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 1 of 1 · 1 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 59062-2200-4 59062220004 45.5 g in 1 APPLICATOR (59062-2200-4) 45.5 g 2013-06-21 0000-00-00 No No Current