Hampton SPF 15 UV-Advanced Sunscreen

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Hampton SPF 15 UV-Advanced Sunscreen
Generic name
HOMOSALATE 7.50% OCTISALATE 5.00% AVOBENZONE 3.00%
Manufacturer
S&C Hampton Sun LLC
Product type
HUMAN OTC DRUG
SPL set ID
1659a681-6cf8-45ba-b1f8-e330eee3b9d4
SPL ID
51cca883-1b7f-d793-e063-6294a90a6d00
Version
2
Effective date
2026-05-14
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:14:31
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Warnings For external use only. Flammable : Do not use white smoking or near heat or flame. Do not use on damaged or broken skin. When using this product ■ keep out of eyes. Rinse eyes with water to remove. Stop use and ask a doctor if rash occurs.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.