Home NDC 87170-021 Hampton Sun SPF 70 Kids
Product NDC 87170-021
11-digit product format 871700021
Labeler code 87170
Product ID 87170-021_521ae910-1b9b-5ed0-e063-6294a90ad152
Type HUMAN OTC DRUG
Nonproprietary name Avobenzone, Humosalate, Octisalate, Octocrylene
Dosage form SPRAY
Route TOPICAL
Labeler S&C Hampton Sun LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-06-25
Substance HOMOSALATE; OCTOCRYLENE; OCTISALATE; AVOBENZONE
Active strength 15; 10; 5; 3 g/100g; g/100g; g/100g; g/100g
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 SPF 70 Kids
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE 15 g/100g OCTOCRYLENE 10 g/100g OCTISALATE 5 g/100g AVOBENZONE 3 g/100g
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 87170-021-05 Hampton Sun SPF 70 Kids 142 g in 1 CAN SPRAY 142 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 87170-021-05 87170002105 142 g in 1 CAN (87170-021-05) 142 g 2022-06-25 No No Current