Hampton Sun SPF50 Mineral Face 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 Sun SPF50 Mineral Face Sunscreen
Generic name
HOMOSALATE 7.5%, OCTISALATE 5.00%, AVOBENZONE 3.00%
Manufacturer
S&C Hampton Sun LLC
Product type
HUMAN OTC DRUG
SPL set ID
f1c5310b-c43b-475d-8a50-d55759ad3164
SPL ID
51a5c787-c3be-9138-e063-6294a90a747b
Version
2
Effective date
2026-05-12
Source export date
2026-11-06
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/39f3c0903357a80632a5484c9d6a804272f4b297080aa9c5a01a84db133f7a03/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 08:04:03
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 For external use only. 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.