FDA.reportPublic FDA data

Sensible SPF 32 Mineral Sunscreen

Product NDC
73369-1501
11-digit product format
733691501
Labeler code
73369
Product ID
73369-1501_ecbe8009-e691-c3c8-e053-2995a90a99bc
Type
HUMAN OTC DRUG
Nonproprietary name
Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
Kabana Skin Care
Application
part352
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2022-04-01
Marketing end
0000-00-00
Substance
ZINC OXIDE
Active strength
25 g/100g
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct73369-1501IInactivated by FDA2026-10-05
excluded packagepackage73369-150173369-1501-1IInactivated by FDA2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage73369-1501-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage73369-1501-1f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73369-1501-12025-07-29C16284748780-13b156c62-2d48-fb37-e063-e6dba90a4e07dd98a2c3-3bcb-15b0-e053-2a95a90a9c37

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73369-1501-1Sensible SPF 32 Mineral Sunscreen85 g in 1 TUBECREAM854

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73369-1501SENSIBLE SPF 32 MINERAL SUNSCREEN (ZINC OXIDE) CREAM [KABANA SKIN CARE]4Legacy NDC, 1 package rows20241030_dd98a2c3-3bcb-15b0-e053-2a95a90a9c37.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73369-1501-17336915010185 g in 1 TUBE (73369-1501-1) 85 g2022-04-010000-00-00NoNoCurrent