Home NDC 62217-013-11 Fruit of the Earth
Product NDC 62217-013
Requested package NDC 62217-013-11
11-digit product format 622170013
Labeler code 62217
Product ID 62217-013_503ab067-0fe8-3d2c-e054-00144ff88e88
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone
Dosage form LOTION
Route TOPICAL
Labeler Fruit of the Earth, Inc.
Application part352
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-05-23
Substance AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE
Active strength 20; 90; 75; 50; 50; 15 mg/mL; mg/mL; 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
Brand name suffix Block Up Kids SPF 50 Moisturizing Sunscreen
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE 20 mg/mL HOMOSALATE 90 mg/mL OCTINOXATE 75 mg/mL OCTISALATE 50 mg/mL OXYBENZONE 50 mg/mL OCTOCRYLENE 15 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 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 62217-013-11 Fruit of the EarthBlock Up Kids SPF 50 Moisturizing Sunscreen 237 mL in 1 BOTTLE LOTION 237 1 62217-013-15 Fruit of the EarthBlock Up Kids SPF 50 Moisturizing Sunscreen 177 mL in 1 TUBE LOTION 177 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62217-013 FRUIT OF THE EARTH BLOCK UP KIDS SPF 50 MOISTURIZING SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [FRUIT OF THE EARTH, INC.] 1 Current NDC, Legacy NDC, 2 package rows 20170524_503a755c-5b86-37d3-e054-00144ff88e88.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 1 of 1 · 1 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 62217-013-11 62217001311 237 mL in 1 BOTTLE (62217-013-11) 237 ml 2017-05-23 0000-00-00 No No Current