Home NDC 87626-001 Sunski Base Camp Face and Body Sunscreen SPF 45
Product NDC 87626-001
11-digit product format 876260001
Labeler code 87626
Product ID 87626-001_597c115b-ceb8-9313-e063-6394a90a0228
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, AVOBENZONE
Dosage form CREAM
Route TOPICAL
Labeler Stewart Charley Ventures, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-01
Substance HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength 150; 50; 30 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 Sunski Base Camp Face and Body Sunscreen SPF 45
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 150 mg/mL OCTISALATE 50 mg/mL AVOBENZONE 30 mg/mL
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 4X49Y0596W Internal UNII lookup G63QQF2NOX Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 87626-001-00 87626000100 1 TUBE in 1 CARTON (87626-001-00) / 75 mL in 1 TUBE 1 tube 2026-09-01 No No Current 87626-001-01 87626000101 1 TUBE in 1 CARTON (87626-001-01) / 150 mL in 1 TUBE 1 tube 2026-09-01 No No Current