Home NDC 49404-154 DR.JART EVERY SUN DAY SUN FLUID
Product NDC 49404-154
11-digit product format 494040154
Labeler code 49404
Product ID 49404-154_2c783ebc-cd45-879f-e063-6394a90a8281
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 2022-12-22
Substance OCTINOXATE; OCTOCRYLENE; HOMOSALATE; AVOBENZONE; OCTISALATE
Active strength 68; 40; 90; 29; 45 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 SUN FLUID
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 68 mg/mL OCTOCRYLENE 40 mg/mL HOMOSALATE 90 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49404-154-01 DR.JART EVERY SUN DAY SUN FLUID 100 mL in 1 CONTAINER LIQUID 100 3 49404-154-01 DR.JART EVERY SUN DAY SUN FLUID 1 in 1 CARTON LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49404-154 DR.JART EVERY SUN DAY SUN FLUID (HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LIQUID [HAVE & BE CO., LTD.] 3 Current NDC, Legacy NDC, 2 package rows 20250126_f06d8f90-f3df-6d76-e053-2a95a90af1f8.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 49404-154-01 49404015401 1 CONTAINER in 1 CARTON (49404-154-01) / 100 mL in 1 CONTAINER 1 container 2022-12-22 0000-00-00 No No Current