Home NDC 84562-510 Tanning Club Everyday Sunscreen SPF 30
Product NDC 84562-510
11-digit product format 845620510
Labeler code 84562
Product ID 84562-510_4f7e16b8-05f6-26cc-e063-6294a90acc5b
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE
Dosage form LOTION
Route TOPICAL
Labeler TANNING CLUB, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-06-27
Substance HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE
Active strength 100; 50; 50; 30 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 Tanning Club Everyday Sunscreen SPF 30
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/mL OCTISALATE 50 mg/mL OCTOCRYLENE 50 mg/mL AVOBENZONE 30 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 84562-510-00 Tanning Club Everyday Sunscreen SPF 30 150 mL in 1 BOTTLE LOTION 150 3 84562-510-03 Tanning Club Everyday Sunscreen SPF 30 88 mL in 1 TUBE LOTION 88 3 84562-510-04 Tanning Club Everyday Sunscreen SPF 30 100 mL in 1 TUBE LOTION 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84562-510 TANNING CLUB EVERYDAY SUNSCREEN SPF 30 (HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE) LOTION [TANNING CLUB, LLC] 1 Current NDC, 3 package rows 20240718_75820400-a5e0-4cf5-8b4f-a52500ce62c3.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 Sample Exclude flag Status 84562-510-00 84562051000 150 mL in 1 BOTTLE (84562-510-00) 150 ml 2024-06-27 No No Current 84562-510-03 84562051003 88 mL in 1 TUBE (84562-510-03) 88 ml 2026-02-12 No No Current 84562-510-04 84562051004 100 mL in 1 TUBE (84562-510-04) 100 ml 2026-04-01 No No Current