Home NDC 63931-4301-1 WL-AAE-ZT-O-391
Product NDC 63931-4301
Requested package NDC 63931-4301-1
11-digit product format 639314301
Labeler code 63931
Product ID 63931-4301_d5c83068-bb7f-47fe-e053-2a95a90aed2e
Type HUMAN OTC DRUG
Nonproprietary name Titanium dioxide, Zinc Oxide
Dosage form LOTION
Route TOPICAL
Labeler Nanophase Technologies Corporation
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2018-10-16
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 1 g/g; g/g
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63931-4301-1 WL-AAE-ZT-O-391 150000 g in 1 DRUM LOTION 150000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63931-4301 WL-AAE-ZT-O-391 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [NANOPHASE TECHNOLOGIES CORPORATION] 3 Legacy NDC, 1 package rows 20220118_77bd9885-55a2-dfae-e053-2991aa0abbe1.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63931-4301-1 63931430101 150000 g in 1 DRUM (63931-4301-1) 150000 g 2018-10-16 0000-00-00 No No Current