Hampton Sun SPF 30 Broad Spectrum Sunscreen Lotion (IS0022-AL)

Manufacturer
S&C Hampton Sun LLC | Inspec Solutions
Effective date
2026-04-22
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:54:45

Label at a glance#

ProductBroad Spectrum Sunscreen SPF 30
Active ingredientOCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE
Label structure7 sections

Indications and uses

Uses ■ helps prevent sunburn

Dosage and administration

Directions apply 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 meas...

Label contents#

Full prescribing information#

Active Ingredeints                Purpose

OTC - ACTIVE INGREDIENT SECTION

Octocrylene - 10.00 %            Sunscreen
Homosalate - 10.00 %            Sunscreen
octisalate - 5-00 %                 Sunscreen
AvohenTone 3 00 %                Sunscreen

Uses

INDICATIONS & USAGE SECTION

Uses ■ helps prevent sunburn

Keep out of reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Polson Control Center right away.

Warnings For external use only.

WARNINGS SECTION


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.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions apply 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.

Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice
BenzvlAlcohol
Caprylic/Capric TrigLyceride
carbomer
Chlorphenesin
Diethylhexyl
Svrinsvlidenemalonate
Disodium EDTA
EthvlhexvlPalmitate
Fragrance
Polyamide 8
Polyoxyethylene Oleyl Ether
Sodium Ascorbyl Phosphate
Sorbitol
TocopherolAcetate
Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87170-007-04Broad Spectrum Sunscreen SPF 30118 mL in 1 BOTTLELOTION1183
87170-007-10Broad Spectrum Sunscreen SPF 30946 mL in 1 BOTTLELOTION9463

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87170-00787170-007-10, 87170-007-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-01-27monthly-update2026-06-03 17:53:15

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
Broad Spectrum Sunscreen SPF 30OCTOCRYLENE 10% HOMOSALATE 10% OCTISALATE 5 % AVOBENZONE 3%S&C Hampton Sun LLCe6103de6-1d80-46fd-b9d4-893f60941def2026-04-22WarningsExact identifier
ndc (package): 87170-007-04
ndc (package): 87170-007-10
ndc (product): 87170-007
ndc11 (package): 87170000704
ndc11 (package): 87170000710
spl id: 50122958-5ad9-0ea8-e063-6394a90a443b
spl set id: e6103de6-1d80-46fd-b9d4-893f60941def

Reported adverse events (FAERS/openFDA)#

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