Home NDC 49404-307 DR.JART EVERY SUN DAY SUN FLUID
Product NDC 49404-307
11-digit product format 494040307
Labeler code 49404
Product ID 49404-307_2d82a7ff-8d4d-02d2-e063-6394a90a2347
Type HUMAN OTC DRUG
Nonproprietary name homosalate, octinoxate, octisalate, octocrylene, avobenzone
Dosage form LIQUID
Route TOPICAL
Labeler Have & Be Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-11
Marketing end 2027-11-30
Substance OCTOCRYLENE; HOMOSALATE; OCTINOXATE; AVOBENZONE; OCTISALATE
Active strength 40; 90; 68; 29; 45 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
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 SUN FLUID Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 40 mg/mL HOMOSALATE 90 mg/mL OCTINOXATE 68 mg/mL AVOBENZONE 29 mg/mL OCTISALATE 45 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
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 49404-307-01 DR.JART EVERY SUN DAY SUN FLUID 1 in 1 CARTON LIQUID 1 3 49404-307-01 DR.JART EVERY SUN DAY SUN FLUID 100 mL in 1 BOTTLE LIQUID 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49404-307 DR.JART EVERY SUN DAY SUN FLUID (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LIQUID [HAVE & BE CO., LTD.] 3 Current NDC, 2 package rows 20250209_02a72c6d-da42-14b2-e063-6394a90af5cb.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 109 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 49404-307-01 49404030701 1 BOTTLE in 1 CARTON (49404-307-01) / 100 mL in 1 BOTTLE 1 bottle 2023-08-11 2027-11-30 No No Historical