BROAD SPECTRUM SUNSCREEN SPF 30- octocrylene 10% homosalate 10% octisalate 5 % avobenzone 3% lotion

Broad Spectrum Sunscreen SPF 30 by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredeints                Purpose

Octocrylene - 10.00 %            Sunscreen
Homosalate - 10.00 %            Sunscreen
octisalate - 5-00 %                 Sunscreen
AvohenTone 3 00 %                Sunscreen

PURPOSE

Uses

Uses ■ helps prevent sunburn

Keep out of reach of children. 

if swallowed, get medical help or contact a Polson Control Center right away.

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.

Directions

Directions apply 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.

Ingredients

Aloe Barbadensis Leaf Juice
BenzvlAlcohol
Caprylic/Capric TrigLyceride
carbomer
Chlorphenesin
Diethylhexyl
Svrinsvlidenemalonate
Disodium EDTA
EthvlhexvlPalmitate
Fragrance
Polyamide 8
Polyoxyethylene Oleyl Ether
Sodium Ascorbyl Phosphate
Sorbitol
TocopherolAcetate
Triethanolamine

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BROAD SPECTRUM SUNSCREEN SPF 30 
octocrylene 10% homosalate 10% octisalate 5 % avobenzone 3% lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87170-007
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
ALOE (UNII: V5VD430YW9)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
CARBOMER (UNII: 0A5MM307FC)
CHLORPHENESIN (UNII: I670DAL4SZ)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
FRAGRANCE ESC 10-740 (UNII: QH92QT9LWR)
POLYAMIDE-8 (4500 MW) (UNII: 77723GV81A)
OLETH-20 (UNII: YTH167I2AG)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87170-007-10	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/27/2026

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 (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions		081030372	manufacture(87170-007)