Home NDC 62217-072 Fruit of the Earth Sun Town City Dark Tanning SPF 8 Sunscreen
Product NDC 62217-072
11-digit product format 622170072
Labeler code 62217
Product ID 62217-072_24b3ce78-5fdc-eda3-e063-6394a90a54b7
Type HUMAN OTC DRUG
Nonproprietary name AVOBENZONE, 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; OCTISALATE; OCTOCRYLENE
Active strength 15; 50; 60 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 Dark Tanning SPF 8 Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 15 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 60 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G63QQF2NOX Internal UNII lookup 4X49Y0596W Internal UNII lookup 5A68WGF6WM Internal UNII lookup
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 62217-072-11 Fruit of the Earth Sun Town City Dark Tanning SPF 8 Sunscreen 237 mL in 1 BOTTLE LOTION 237 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62217-072 FRUIT OF THE EARTH SUN TOWN CITY DARK TANNING SPF 8 SUNSCREEN (AVOBENZONE, OCTISALATE, OCTOCRYLENE) LOTION [FRUIT OF THE EARTH, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241019_c7aa1e58-f7b3-6b7f-e053-2995a90a957c.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 62217-072-11 62217007211 237 mL in 1 BOTTLE (62217-072-11) 237 ml 2019-12-09 0000-00-00 No No Current