Home NDC 59062-0120 BABYGANICS SPF 50 Plus SUNSCREEN
Product NDC 59062-0120
11-digit product format 590620120
Labeler code 59062
Product ID 59062-0120_0bd9880a-6b33-495b-a58e-7a5e65cbac4a
Type HUMAN OTC DRUG
Nonproprietary name ZINC OXIDE, OCTISALATE, and OCTOCRYLENE
Dosage form SPRAY
Route TOPICAL
Labeler KAS Direct LLC dba Babyganics
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-01
Marketing end 2026-12-31
Substance ZINC OXIDE; OCTISALATE; OCTOCRYLENE
Active strength 112; 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 BABYGANICS SPF 50 Plus SUNSCREEN Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 112 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 4X49Y0596W Internal UNII lookup 5A68WGF6WM 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 59062-0120-1 BABYGANICS SPF 50 Plus SUNSCREEN 177 mL in 1 BOTTLE, DISPENSING SPRAY 177 4 59062-0120-6 outdoor essentials 177 mL in 1 BOTTLE, SPRAY SPRAY 177 mL 112 mg in 1mL 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59062-0120 BABYGANICS SPF 50 PLUS SUNSCREEN (ZINC OXIDE, OCTISALATE, AND OCTOCRYLENE) SPRAY [KAS DIRECT LLC DBA BABYGANICS] 4 Current NDC, Legacy NDC, 1 package rows 20241225_4075f9dc-c25f-434f-a3fc-a7f896295c3d.zip 59062-0120 OUTDOOR ESSENTIALS (ZINC OXIDE, OCTOCRYLENE, AND OCTISALATE) KIT [KAS DIRECT LLC DBA BABYGANICS] 2 Current NDC, Legacy NDC 20211023_93ef5b1b-e4f4-4c86-a395-c19861866c3e.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 59062-0120-1 59062012001 177 mL in 1 BOTTLE, DISPENSING (59062-0120-1) 177 ml 2019-07-01 2026-12-31 No No Current 59062-0120-6 59062012006 177 mL in 1 BOTTLE, SPRAY 177 ml Historical