Home NDC 87170-010 HAMPTON SUN SPF50 SUNSHIELD BODY GLOW
Product NDC 87170-010
11-digit product format 871700010
Labeler code 87170
Product ID 87170-010_49d8d864-063b-8c16-e063-6294a90a279a
Type HUMAN OTC DRUG
Nonproprietary name Homosalate 10% Octocrylene 10% Avobenzone 3% Octicalate 5%
Dosage form OIL
Route TOPICAL
Labeler S&C Hampton Sun LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-01
Substance HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
Active strength 10; 10; 3; 5 g/100mL; g/100mL; g/100mL; g/100mL
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 HAMPTON SUN SPF50 SUNSHIELD BODY GLOW
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 10 g/100mL OCTOCRYLENE 10 g/100mL AVOBENZONE 3 g/100mL OCTISALATE 5 g/100mL
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 87170-010-04 HAMPTON SUN SPF50 SUNSHIELD BODY GLOW 100 mL in 1 TUBE OIL 100 2
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 87170-010-04 87170001004 100 mL in 1 TUBE (87170-010-04) 100 ml 2026-01-01 No No Current