kids SPF 50plus sunscreen continuous

Product NDC
59062-0175
Requested package NDC
59062-0175-6
11-digit product format
590620175
Labeler code
59062
Product ID
59062-0175_bb064d2a-af0b-49b5-9141-998c8c4b6295
Type
HUMAN OTC DRUG
Nonproprietary name
ZINC OXIDE and OCTISALATE
Dosage form
SPRAY
Route
TOPICAL
Labeler
KAS Direct LLC dba BabyGanics
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2018-12-15
Marketing end
0000-00-00
Substance
ZINC OXIDE; OCTISALATE
Active strength
150 mg/g; mg/g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59062-017559062-0175-6DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59062-0175KIDS SPF 50PLUS SUNSCREEN CONTINUOUS (ZINC OXIDE AND OCTISALATE) SPRAY [KAS DIRECT LLC DBA BABYGANICS]3Legacy NDC20241222_b83ffd3b-b7fa-488f-9103-70b6bba6ae7f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59062-0175-659062017506170 g in 1 CAN (59062-0175-6) 170 g2018-12-150000-00-00NoNoCurrent