Home NDC 70618-040 Sun Project Moisture
Product NDC 70618-040
11-digit product format 706180040
Labeler code 70618
Product ID 70618-040_485049b1-9fd6-c1f2-e063-6394a90aaf5d
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, OCTOCRYLENE, BUTYL METHOXYDIBENZOYLMETHANE
Dosage form CREAM
Route TOPICAL
Labeler THANK YOU FARMER CO., LTD
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-09-16
Substance OCTISALATE; OCTINOXATE; OCTOCRYLENE; AVOBENZONE; HOMOSALATE
Active strength 2.25; 3.4; 2; 1.35; 4.5 g/50mL; g/50mL; g/50mL; g/50mL; g/50mL
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 Sun Project Moisture
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTISALATE 2.25 g/50mL OCTINOXATE 3.4 g/50mL OCTOCRYLENE 2 g/50mL AVOBENZONE 1.35 g/50mL HOMOSALATE 4.5 g/50mL
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 70618-040-01 Sun Project Moisture 50 mL in 1 TUBE CREAM 50 3 70618-040-02 Sun Project Moisture 60 in 1 CARTON CREAM 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70618-040 SUN PROJECT MOISTURE (HOMOSALATE, ETHYLHEXYL METHOXYCINNAMATE, ETHYLHEXYL SALICYLATE, OCTOCRYLENE, BUTYL METHOXYDIBENZOYLMETHANE) CREAM [THANK YOU FARMER CO., LTD] 2 Current NDC, 2 package rows 20240917_20a83f02-d851-4aac-e063-6394a90ae1a6.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 Sample Exclude flag Status 70618-040-01 70618004001 50 mL in 1 TUBE 50 ml Historical 70618-040-02 70618004002 60 TUBE in 1 CARTON (70618-040-02) / 50 mL in 1 TUBE (70618-040-01) 60 tube 2024-09-16 No No Current