Home NDC 49404-306 DR.JART EVERY SUN DAY MINERAL SUN SCREEN
Product NDC 49404-306
11-digit product format 494040306
Labeler code 49404
Product ID 49404-306_2d828e05-0be7-79cb-e063-6294a90a7716
Type HUMAN OTC DRUG
Nonproprietary name titanium dioxide, zinc oxide
Dosage form CREAM
Route TOPICAL
Labeler Have & Be Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-11
Marketing end 2027-12-31
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 41; 115 mg/mL; mg/mL
NDC exclude flag No
Current FDA listing Yes 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 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base DR.JART EVERY SUN DAY MINERAL SUN SCREEN Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 41 mg/mL ZINC OXIDE 115 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49404-306-01 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 50 mL in 1 TUBE CREAM 50 4 49404-306-01 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 1 in 1 CARTON CREAM 1 4 49404-306-02 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 5 mL in 1 TUBE CREAM 5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49404-306 DR.JART EVERY SUN DAY MINERAL SUN SCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HAVE & BE CO., LTD.] 4 Current NDC, 3 package rows 20250209_02a671ed-485d-d6b7-e063-6394a90ad4af.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 49404-306-01 49404030601 1 TUBE in 1 CARTON (49404-306-01) / 50 mL in 1 TUBE 1 tube 2023-08-11 2027-12-31 No No Historical 49404-306-02 49404030602 5 mL in 1 TUBE 5 ml Historical