FDA.reportPublic FDA data

HAMPTON SUN

Manufacturer
Hampton Sun | Inspec Solutions LLC.
Effective date
2025-10-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:38:59

Label at a glance#

ProductHAMPTON SUN
Active ingredientOCTINOXATE, OXYBENZONE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Octinoxate – 4.00%

Oxybenzone - 2.00%

OTC - PURPOSE SECTION

Octinoxate – 4.00%..................Sunscreen

Oxybenzone - 2.00%...............Sunscreen

INDICATIONS & USAGE SECTION


Uses • Helps prevent sunburn​

WARNINGS SECTION

Warnings

Skin cancer/Skin Aging alert

For external use only

Do not use on Damage or broken skin

When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION


Stop use and ask a doctor if rash occurs.​

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

• Apply liberally 15 minutes before sun exposure.

• Use water resistant sunscreen if swimming or sweating

• Reapply at least every 2 hours

•​ Children under 6 months of age: ask a doctor

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Aloe Barbadensis Leaf Extract, Benzotriazolyl Dodecyl p-Cresol, C12-15 Alkyl Benzoate, Cyclohexasiloxane, Cyclopentasiloxane

Dimethicone Crosspolymer, Ethylhexyl Palmitate, Fragrance, Hydrogenated Polyisobutene, Hydrolyzed Jojoba Esters, Jojoba Esters, Juglans Regia (Walnut) Seed Oil, Mineral Oil, Sorbitan Olivate, Tocopheryl Acetate, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SPF 4 OILSPF 4 OIL

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130184573000015GTIN-13: 0184573000015
EAN-13: 0184573000015
GTIN-12: 184573000015
UPC-A: 184573000015
GTIN storage (14 digits): 00184573000015		2019-06-01_101319.jpg

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87170-00187170-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOEV5VD430YW9IACT
BENZOTRIAZOLYL DODECYL P-CRESOL298PX4M11XIACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
WALNUT OILY0P3555R51IACT
MINERAL OILT5L8T28FGPIACT
ETHYLHEXYL PALMITATE2865993309IACT
SORBITAN OLIVATEMDL271E3GRIACT
C12-15 ALCOHOLS2C8M6XLB5CIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS)CH428W5O62IACT
OCTINOXATE4Y5P7MUD51ACTIB
OXYBENZONE95OOS7VE0YACTIB

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
4f82ad62-e47f-54b1-e063-6394a90a7be5a5e7efb4-cf14-4ffa-ae7b-470653d8e6f62026-04-15WarningsExact identifier
spl set id: a5e7efb4-cf14-4ffa-ae7b-470653d8e6f6

Reported adverse events (FAERS/openFDA)#

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