HAMPTON SUN SPF 30 MINERAL- zinc oxide 7.20% titanium dioxide 4.00% spray

Hampton Sun SPF 30 Mineral by

Drug Labeling and Warnings

Hampton Sun SPF 30 Mineral by is a Otc medication manufactured, distributed, or labeled by S&C Hampton Sun LLC, Inspec Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Actove Ingredeints                Purpose

Zinc Oxide 7.2%                     Sunscreen

Titanium Dioxide 4%               Sunscreen

PURPOSE

Uses

Uses ■ helps prevent sunburn

DOSAGE & ADMINISTRATION

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
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.

KEEP OUT OF REACH OF CHILDREN

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

Inactive Ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAMPTON SUN SPF 30 MINERAL 
zinc oxide 7.20% titanium dioxide 4.00% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	7.2 g  in 100 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (CI 77891 - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CETYL DIGLYCERYL TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE (3500 MM2/S) (UNII: KB7T6C99UP)
DIMETHICONE (UNII: 92RU3N3Y1O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
FRAGRANCE 13576 (UNII: 5EM498GW35)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN DIMETHICONE (30 CST) (UNII: JF2ZJ6R2WD)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
JOJOBA OIL, RANDOMIZED (UNII: 7F0EV20QYL)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
PROPANEDIOL (UNII: 5965N8W85T)
SILICA (UNII: ETJ7Z6XBU4)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
SODIUM PHYTATE (UNII: 88496G1ERL)
SORBITAN OLIVATE (UNII: MDL271E3GR)
STEARIC ACID (UNII: 4ELV7Z65AP)
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-008-05	142 g in 1 CAN; Type 0: Not a Combination Product	01/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/01/2026

Labeler - S&C Hampton Sun LLC (031880374)

Registrant - Inspec Solutions LLC (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC		081030372	manufacture(87170-008)