Home NDC 65008-007 Sunsorb Reef Safe SPF50
Product NDC 65008-007
11-digit product format 650080007
Labeler code 65008
Product ID 65008-007_4354d16c-e4d4-d163-e063-6394a90aff83
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Zinc Oxide, Octocrylene
Dosage form LOTION
Route TOPICAL
Labeler QS Key West Aloe, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-15
Substance HOMOSALATE; ZINC OXIDE; OCTOCRYLENE
Active strength 100; 57; 50 mg/g; mg/g; mg/g
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 Sunsorb Reef Safe SPF50
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 100 mg/g ZINC OXIDE 57 mg/g OCTOCRYLENE 50 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination V06SV4M95S Internal UNII lookup SOI2LOH54Z Internal UNII lookup 5A68WGF6WM 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 65008-007-06 Sunsorb Reef Safe SPF50 170 g in 1 TUBE LOTION 170 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 65008-007 SUNSORB REEF SAFE SPF50 (HOMOSALATE, ZINC OXIDE, OCTOCRYLENE) LOTION [QS KEY WEST ALOE, LLC] 5 Current NDC, Legacy NDC, 1 package rows 20241210_b4fc7a51-a163-4057-8790-f2111668ec67.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 65008-007-06 65008000706 170 g in 1 TUBE (65008-007-06) 170 g 2019-07-15 0000-00-00 No No Current