Home NDC 62217-079 Fruit of the Earth Sun Town City SPF 30 Sunscreen
Product NDC 62217-079
11-digit product format 622170079
Labeler code 62217
Product ID 62217-079_24c6d867-e7f3-ead2-e063-6394a90a5498
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Dosage form LOTION
Route TOPICAL
Labeler Fruit of the Earth, Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-12-09
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 30; 80; 45; 60 mg/mL; mg/mL; 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 Fruit of the Earth Sun Town City SPF 30 Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 30 mg/mL HOMOSALATE 80 mg/mL OCTISALATE 45 mg/mL OCTOCRYLENE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62217-079-11 Fruit of the Earth Sun Town City SPF 30 Sunscreen 237 mL in 1 BOTTLE LOTION 237 2 62217-079-82 Fruit of the Earth Sun Town City SPF 30 Sunscreen 100 mL in 1 BOTTLE LOTION 100 2 62217-079-83 Fruit of the Earth Sun Town City SPF 30 Sunscreen 44 mL in 1 TUBE LOTION 44 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62217-079 FRUIT OF THE EARTH SUN TOWN CITY SPF 30 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [FRUIT OF THE EARTH, INC.] 2 Current NDC, Legacy NDC, 3 package rows 20241020_c85e5094-d442-55a9-e053-2995a90aed12.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 62217-079-11 62217007911 237 mL in 1 BOTTLE (62217-079-11) 237 ml 2019-12-09 0000-00-00 No No Current 62217-079-82 62217007982 100 mL in 1 BOTTLE (62217-079-82) 100 ml 2019-12-09 0000-00-00 No No Current 62217-079-83 62217007983 44 mL in 1 TUBE (62217-079-83) 44 ml 2019-12-09 0000-00-00 No No Current