Home NDC 49404-153 DR.JART EVERY SUN DAY MINERAL SUN SCREEN
Product NDC 49404-153
11-digit product format 494040153
Labeler code 49404
Product ID 49404-153_47ed472b-224a-5b9a-e063-6394a90a7030
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 2022-12-22
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 115; 41 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 115 mg/mL TITANIUM DIOXIDE 41 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49404-153-01 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 1 in 1 CARTON CREAM 1 5 49404-153-01 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 50 mL in 1 TUBE CREAM 50 5 49404-153-02 DR.JART EVERY SUN DAY MINERAL SUN SCREEN 5 mL in 1 TUBE CREAM 5 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49404-153 DR.JART EVERY SUN DAY MINERAL SUN SCREEN (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [HAVE & BE CO., LTD.] 4 Current NDC, Legacy NDC, 3 package rows 20241227_f06c31b4-da5f-6495-e053-2995a90ae67c.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 49404-153-01 49404015301 1 TUBE in 1 CARTON (49404-153-01) / 50 mL in 1 TUBE 1 tube 2022-12-22 0000-00-00 No No Current 49404-153-02 49404015302 5 mL in 1 TUBE (49404-153-02) 5 ml 2022-12-22 0000-00-00 No No Current