Home NDC 85161-166 Poolside Glow Butter Screen SPF 30 Shimmer sunscreen Butter
Product NDC 85161-166
11-digit product format 851610166
Labeler code 85161
Product ID 85161-166_452bd69e-02c8-fcbd-e063-6394a90ae59b
Type HUMAN OTC DRUG
Nonproprietary name Homosalate , Octocrylene, Octisalate , Avobenzone
Dosage form OIL
Route TOPICAL
Labeler Longway Technology(Guangzhou)Co.,Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-15
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength .03; .15; .05; .1 g/g; g/g; g/g; g/g
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 Poolside Glow Butter Screen SPF 30 Shimmer sunscreen Butter
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AVOBENZONE .03 g/g HOMOSALATE .15 g/g OCTISALATE .05 g/g OCTOCRYLENE .1 g/g
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 85161-166-01 Poolside Glow Butter Screen SPF 30 Shimmer sunscreen Butter 80 g in 1 BOTTLE OIL 80 1
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 85161-166-01 85161016601 80 g in 1 BOTTLE (85161-166-01) 80 g 2026-01-15 No No Current