FDA.reportPublic FDA data

Neutrogena Mineral Beach Defense Active Performance Sunscreen Broad Spectrum SPF 30

Product NDC
69968-0773
Requested package NDC
69968-0773-3
11-digit product format
699680773
Labeler code
69968
Product ID
69968-0773_e4af62e3-d0f1-4c73-e053-2995a90aba99
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide, Zinc Oxide
Dosage form
LOTION
Route
TOPICAL
Labeler
Johnson & Johnson Consumer Inc.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2022-10-04
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE; ZINC OXIDE
Active strength
65 mg/mL; mg/mL
NDC exclude flag
No
Listing certified through
2023-12-31
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 packagepackage69968-077369968-0773-3DDiscontinued 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
69968-0773NEUTROGENA MINERAL BEACH DEFENSE ACTIVE PERFORMANCE SUNSCREEN BROAD SPECTRUM SPF 30 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [KENVUE BRANDS LLC]4Legacy NDC20241115_e4af6288-89e6-3fb8-e053-2a95a90a12e0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69968-0773-36996807730388 mL in 1 TUBE (69968-0773-3) 88 ml2022-10-040000-00-00NoNoCurrent