Home NDC 62217-043 FOTE CABANA BEACH CLUB WITH BLOOD ORANGE AND ESSENTIAL OILS SPF 8 DRY TANNING SUNSCREEN
Product NDC 62217-043
11-digit product format 622170043
Labeler code 62217
Product ID 62217-043_24b35fac-b6cc-2398-e063-6394a90af56c
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler FRUIT OF THE EARTH, INC.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-01-15
Substance HOMOSALATE; OCTISALATE
Active strength 70; 50 mg/g; mg/g
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 FOTE CABANA BEACH CLUB WITH BLOOD ORANGE AND ESSENTIAL OILS SPF 8 DRY TANNING SUNSCREEN
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 70 mg/g OCTISALATE 50 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup 4X49Y0596W Internal UNII lookup
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 62217-043-37 FOTE CABANA BEACH CLUB WITH BLOOD ORANGE AND ESSENTIAL OILS SPF 8 DRY TANNING SUNSCREEN 156 g in 1 CAN AEROSOL, SPRAY 156 3 62217-043-74 FOTE CABANA BEACH CLUB WITH BLOOD ORANGE AND ESSENTIAL OILS SPF 8 DRY TANNING SUNSCREEN 76.5 g in 1 CAN AEROSOL, SPRAY 76.5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62217-043 FOTE CABANA BEACH CLUB WITH BLOOD ORANGE AND ESSENTIAL OILS SPF 8 DRY TANNING SUNSCREEN (HOMOSALATE, OCTISALATE) AEROSOL, SPRAY [FRUIT OF THE EARTH, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20241019_13325a2a-f7f8-4019-acbb-205fd5dd13a5.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 62217-043-37 62217004337 156 g in 1 CAN (62217-043-37) 156 g 2019-01-15 0000-00-00 No No Current 62217-043-74 62217004374 76.5 g in 1 CAN (62217-043-74) 76.5 g 2019-04-03 0000-00-00 No No Current