FDA.reportPublic FDA data

Natural Defense Finishing Powder

Product NDC
31645-219
Requested package NDC
31645-219-02
11-digit product format
316450219
Labeler code
31645
Product ID
31645-219_e6134920-9d74-c577-e053-2a95a90a96f0
Type
HUMAN OTC DRUG
Nonproprietary name
Octinoxate, Oxybenzone, Titanium Dioxide, Zinc Oxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Physicians Formula
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-01-01
Marketing end
0000-00-00
Substance
OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
5 mg/g; mg/g; mg/g; mg/g
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 packagepackage31645-21931645-219-02DDiscontinued by firm2026-10-05

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
31645-219-022023-12-28C16284748780-10191ceaa-64cf-198a-e063-dbdaa90aec3eNatural Defense Finishing Powder
31645-219-022023-07-28C16284748780-10191ceaa-64cf-198a-e063-dbdaa90aec3eNatural Defense Finishing Powder

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
31645-219-02316450219021 CONTAINER in 1 CARTON (31645-219-02) > 10 g in 1 CONTAINER (31645-219-01) 1 container2021-01-010000-00-00NoNoCurrent