FDA.reportPublic FDA data

Hampton Sun SPF50 Mineral Face Stick (.45oz) IS0382-HS

Manufacturer
S&C Hampton Sun LLC | Inspec Solutions LLC
Effective date
2026-05-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:57:06

Label at a glance#

ProductHampton Sun SPF50 Mineral Face Sunscreen
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

Uses ■ helps prevent sunburn

Label contents#

Full prescribing information#

Active Ingredeints

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 14.69%

Uses

INDICATIONS & USAGE SECTION

Uses ■ helps prevent sunburn

DOSAGE & ADMINISTRATION SECTION

Directionsapply liberally to cool, dry skin
15 minutes before sun exposure • reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying • at least every 2
hours • Sun Protection Measures. Spending time
in the sun increases your risk of skin cancer and
early skin aging. To decrease this risk, regularly
use a sunscreen with a broad spectrum SPF of 15
or higher and other sun protection measures
including: • limit time in the sun,especially from
10 a.m. - 2. p.m. • wear a long-sleeve shirts,
pants, hats, and sunglasses. • children under 6
months: Ask a doctor.
■ do not spray
directly Into face. Spray on hands then apply to face ■ use In
well-ventilated area.
Hold container 6-8 inches from the skin to apply

Warnings

WARNINGS SECTION

For external use only.
Do not useon damaged or broken skin.
When using this product■ keep out of eyes. Rinse eyes with water
to remove.
Stop use and ask a doctor ifrash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.if swallowed, get medical
help or contact a Polson Control Center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Triethoxycaprylylsilane 

Octyldodecanol

Dibutyl Lauroyl Glutamide
Dibutyl Ethylhexanoyl Glutamide
Caprilic/Capric Triglyceride
C12-15 Alkyl Benzoate
VP/Hexadecene Copolymer
Butyloctyl Salicylate
Ethylhexyl Methoxycrylene
Simmondsia Chinensis (Jojoba) Seed Oil
Vitis Vinifera (Grape) Seed Oil
Butyrospermum Parkii (Shea) Oil
Tocopheryl Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87170-012-01Hampton Sun SPF50 Mineral Face Sunscreen13 g in 1 CONTAINERSTICK132

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87170-01287170-012-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
OCTYLDODECANOL461N1O614YIACT
DIBUTYL LAUROYL GLUTAMIDE3V7K3IA58XIACT
DIBUTYL ETHYLHEXANOYL GLUTAMIDE0IAF2L30VSIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
VP/HEXADECENE COPOLYMERKFR5QEN0N9IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
ETHYLHEXYL METHOXYCRYLENES3KFG6Q5X8IACT
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL724GKU717MIACT
VITIS VINIFERA (GRAPE) SEED OIL930MLC8XGGIACT
BUTYROSPERMUM PARKII (SHEA) OILO88E196QRFIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
ZINC OXIDESOI2LOH54ZACTIM

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hampton Sun SPF50 Mineral Face SunscreenHOMOSALATE 7.5%, OCTISALATE 5.00%, AVOBENZONE 3.00%S&C Hampton Sun LLCf1c5310b-c43b-475d-8a50-d55759ad31642026-05-12WarningsExact identifier
ndc (package): 87170-012-01
ndc (product): 87170-012
ndc11 (package): 87170001201
spl id: 51a5c787-c3be-9138-e063-6294a90a747b
spl set id: f1c5310b-c43b-475d-8a50-d55759ad3164

Reported adverse events (FAERS/openFDA)#

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