HAMPTON SUN SPF 50- avobenzone 3.00 % octisalate 5.00 % homosalate 10.00 % spray

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Avobenzone 3.00 %
Octisalate 5.00 %
Homosalate 10.00 %

WHEN USING

When using this product:

Apply liberally15 min before sun exposure and as needed. 

Reapply after 80 min of sweeming and sweating,

immedialy after towel drying, at least every two hours

keep out of eyes. Rinse with water to remove.

Keep away from face to avoid breathing it.

Do not puncture or incinerate, Contents under pressure

Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

DOSAGE & ADMINISTRATION

WARNINGS

PURPOSE

Purpose

Sunscreen

Uses:

Helps prevent sunburn, higher SPF gives more sun protection

STOP USE

Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

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

INACTIVE INGREDIENT

Aloe Barbadensis Leaf Extract
Butyloctyl Salicylate
Camellia Sinensis Leaf Extract
Cocos Nucifera (Coconut) Fruit Extract
DL-Alpha-tocopheryl-Acetate
Ethanol
Fragrance
Glycerin
Helianthus Annuus (Sunflower) Seed Oil
Leuconostoc/Radish Root Ferment Filtrate
Mineral Oil
Oryza Sativa (Rice) Bran Oil
Phenoxyethanol
Polyester-8
Propylene Glycol
Sodium Hyaluronate
VA/Butyl Maleate/Isobornyl Acrylate Copolymer
Vitis Vinifera (Grape) Seed Extract
Water

WHEN USING

keep out of eyes. Rinse with water to remove.

Keep away from face to avoid breathing it.

Do not puncture or incinerate, Contents under pressure

Do not store at temperature above 120⁰F

Stop use and ask a doctor if rash occurs.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAMPTON SUN SPF 50 
avobenzone 3.00 % octisalate 5.00 % homosalate 10.00 % spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0)
COCOS NUCIFERA (COCONUT) FRUIT JUICE (UNII: AMN6S4M09G)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
ALCOHOL (UNII: 3K9958V90M)
FRAGRANCE 13576 (UNII: 5EM498GW35)
GLYCERIN (UNII: PDC6A3C0OX)
SUNFLOWER OIL (UNII: 3W1JG795YI)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
MINERAL OIL (UNII: T5L8T28FGP)
RICE BRAN OIL (UNII: LZO6K1506A)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
VITIS VINIFERA (GRAPE) SEED EXTRACT (UNII: RDS2V6DVY5)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-020-05	142 g in 1 CAN; Type 0: Not a Combination Product	06/25/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	06/25/2022

Labeler - S&C Hampton Sun LLC (031880374)

Registrant - Inspec Solutions (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(87170-020)