Hampton Sun SPF 50 Mineral

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 SPF 50 Mineral
Generic name
ZINC OXIDE 19.5% TITANIUM DIOXIDE 4.00%
Manufacturer
S&C Hampton Sun LLC
Product type
HUMAN OTC DRUG
SPL set ID
d6c33436-042e-44e8-8b55-98be6e246879
SPL ID
4a2a358f-7485-c00e-e063-6394a90ab0a6
Version
2
Effective date
2026-02-06
Source export date
2026-10-30
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:59:59
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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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.