HAMPTON SUN SPF50 MINERAL FACE SUNSCREEN- homosalate 7.5%, octisalate 5.00%, avobenzone 3.00% stick

Drug Labeling and Warnings

Drug Details [pdf]

Purpose    Sunscreen

Active Ingredeints

Zinc Oxide 14.69%

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

For external use only.
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

Triethoxycaprylylsilane 

Octyldodecanol

Dibutyl Lauroyl Glutamide
Dibutyl Ethylhexanoyl Glutamide
Caprilic/Capric Triglyceride
C12-15 Alkyl Benzoate
VP/Hexadecene Copolymer
Butyloctyl Salicylate
Ethylhexyl Methoxycrylene
Simmondsia Chinensis (Jojoba) Seed Oil
Vitis Vinifera (Grape) Seed Oil
Butyrospermum Parkii (Shea) Oil
Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAMPTON SUN SPF50 MINERAL FACE SUNSCREEN 
homosalate 7.5%, octisalate 5.00%, avobenzone 3.00% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	14.69 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
OCTYLDODECANOL (UNII: 461N1O614Y)
DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
VP/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL (UNII: 724GKU717M)
VITIS VINIFERA (GRAPE) SEED OIL (UNII: 930MLC8XGG)
BUTYROSPERMUM PARKII (SHEA) OIL (UNII: O88E196QRF)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-012-01	13 g in 1 CONTAINER; Type 0: Not a Combination Product	12/01/2025

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

Labeler - S&C Hampton Sun LLC (031880374)

Registrant - Inspec Solutions LLC (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC		081030372	manufacture(87170-012)