HAMPTON SUN SPF 8 SUNSCREEN GEL

HAMPTON SUN by

Drug Labeling and Warnings

HAMPTON SUN by is a Otc medication manufactured, distributed, or labeled by Hampton Sun, Inspec Solutions LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAMPTON SUN- octinoxate, octisalate, oxybenzone spray 
Hampton Sun

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HAMPTON SUN SPF 8 SUNSCREEN GEL

Active Ingredients:

Octinoxate - 7.50%

Octisalate - 5.00%

Oxybenzone - 3.00%

Octinoxate - 7.50% .....................Sunscreen.

Octisalate - 5.00% ......................Sunscreen.​

Oxybenzone - 3.00% ..................Sunscre.en.​

Use helps prevent sunburn.

Warnings

Skin cancer/Skin Aging alert

For external use only

Do noy use on Damage or broken skin

keep out of eyes. Rinse with water to remove. ​

Stop use and ask a doctor if rash occurs.​

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

DIRECTIONS

Apply liberally 15 minutes before sun exposure.

Use a water resistant sunscreen if swimming or sweating.

Reapply at least every 2 hours

Children under 6 months of age: ask a doctor.

Inactive Ingredients:

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

Dimethicone Crosspolymer, Fragrance, Hydrogenated Polyisobutene, Hydrolyzed Jojoba Esters, Jojoba Esters, Juglans Regia (Walnut) Seed Oil, Mineral OilSorbitan Olivate, Tocopheryl Acetatel, Water

HAMPTON SUN 
octinoxate, octisalate, oxybenzone spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	3 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)
ALOE (UNII: V5VD430YW9)
TRIEPOXYCYCLOHEXASILANE (UNII: 066Q83563R)
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
HYDROLYZED JOJOBA ESTERS (POTASSIUM SALTS) (UNII: CH428W5O62)
WALNUT OIL (UNII: Y0P3555R51)
SORBITAN OLIVATE (UNII: MDL271E3GR)
BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X)
MINERAL OIL (UNII: T5L8T28FGP)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-002-01	118 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/27/2025	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/27/2025	12/01/2025

Labeler - Hampton Sun (031880374)

Registrant - Inspec Solutions LLC. (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC.		081030372	manufacture(87170-002)

Revised: 4/2026

Document Id: 4f7265a7-6181-4ee4-e063-6394a90aee51

34390-5

Set id: ba082453-f7f0-48ca-b7bd-6d17a67b6711

Version: 3

Effective Time: 20260414