Home NDC 51060-359-01 BB tinted treatment primer Broad Spectrum SPF 30 Sunscreen
Product NDC 51060-359
Requested package NDC 51060-359-01
11-digit product format 510600359
Labeler code 51060
Product ID 51060-359_9233328c-e728-450c-b00b-599abab04352
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE AND ZINC OXIDE
Dosage form LIQUID
Route TOPICAL
Labeler Tarte, Inc.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2012-09-01
Marketing end 0000-00-00
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 46 mg/mL; mg/mL
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 51060-359-01 BB tinted treatment primer Broad Spectrum SPF 30 Sunscreen light-medium 30 mL in 1 TUBE LIQUID 30 2 51060-359-01 BB tinted treatment primer Broad Spectrum SPF 30 Sunscreen light-medium 1 in 1 CARTON LIQUID 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51060-359 BB TINTED TREATMENT PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN FAIR (TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID BB TINTED TREATMENT PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN LIGHT (TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID BB TINTED TREATMENT PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN MEDIUM (TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID BB TINTED TREATMENT PRIMER BROAD S .......IUM DIOXIDE AND ZINC OXIDE) LIQUID BB TINTED TREATMENT PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN RICH HONEY (TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID BB TINTED TREATMENT PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN MAHOGANY HONEY (TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID BB TINTED TREATMENT PRIMER BROAD SPECTRUM SPF 30 SUNSCREEN ESPRESSO (TITANIUM DIOXIDE AND ZINC OXIDE) LIQUID [TARTE, INC.] 2 Legacy NDC, 2 package rows 20220817_500db28a-40f0-4d5c-aa82-baeb4b466ef3.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51060-359-01 51060035901 1 TUBE in 1 CARTON (51060-359-01) > 30 mL in 1 TUBE 1 tube 2012-09-01 0000-00-00 No No Current