Hampton Sun SFP 30 Mineral Spray (IS0325-HSF)

Manufacturer
S&C Hampton Sun LLC | Inspec Solutions LLC
Effective date
2026-01-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:35:16

Label at a glance#

ProductHampton Sun SPF 30 Mineral
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure7 sections

Indications and uses

Uses ■ helps prevent sunburn

Label contents#

Full prescribing information#

Actove Ingredeints                Purpose

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 7.2%                     Sunscreen

Titanium Dioxide 4%               Sunscreen

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

Warnings
For external use only.
Flammable: Do not use white smoking or near heat or flame.
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

Aloe Barbadensis Leaf Juice
Caprylic/Capric Triglyceride
Caprylyl Glycol
Cetyl Diglyceryl Tris(Trimethylsiloxy)silylethyl Dimethicone
Dimethicone
Ethylhexylglycerin
Fragrance
Glycerin
Hydrogen Dimethicone
Isopropyl Myristate
Jojoba Esters
Pentylene Glycol
Polyhydroxystearic Acid
Propanediol
Silica
Sodium Chloride
Sodium Hyaluronate
Sodium Phytate
Sorbitan Olivate
Stearic Acid
Synthetic Beeswax
Tocopheryl Acetate
Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87170-008-05Hampton Sun SPF 30 Mineral142 g in 1 CANSPRAY1422

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87170-00887170-008-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

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 SPF 30 MineralZINC OXIDE 7.20% TITANIUM DIOXIDE 4.00%S&C Hampton Sun LLCb8ee428e-07d3-4c6c-853c-cfbe3e4002d92026-01-28WarningsExact identifier
ndc (package): 87170-008-05
ndc (product): 87170-008
ndc11 (package): 87170000805
spl id: 49731d35-e91b-ce13-e063-6294a90ace5d
spl set id: b8ee428e-07d3-4c6c-853c-cfbe3e4002d9

Reported adverse events (FAERS/openFDA)#

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