HAMPTON SUN SPF 70 KIDS- avobenzone, humosalate, octisalate, octocrylene spray

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Avobenzone 3.0%

Homosalate 15%

Octisalate 5%

Octocrylene 10%

PURPOSE

Sunscreen

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 use on damaged or broken skin.
When using this product ■ keep out of eyes. Rinse eyes with water
to remove.
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 Polson Control Center right away.

Inactive Ingredeints

Alcohol
Aloe Barbadensis Leaf Extract
Acrylates/Octylacrylamide Copolymer
Butyloctyl Salicylate
Caprylic/Capric Triglyceride
Diethylhexyl Syringylidenemalonate
Glycerin
Mineral Oil
Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAMPTON SUN SPF 70 KIDS 
avobenzone, humosalate, octisalate, octocrylene spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-021
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	15 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	10 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W)	OCTISALATE	5 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ALOE (UNII: V5VD430YW9)
ACRYLATES/OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
GLYCERIN (UNII: PDC6A3C0OX)
MINERAL OIL (UNII: T5L8T28FGP)
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-021-05	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(87170-021)