SPF 50 DRY TOUCH CONTINUOUS NO FRAGRANCE- homosalate 10.00% octisalate 5.00% avobenzone 3.00% liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredients                 

Homosalate 10.00%
Octisalate 5.00%
Avobenzone 3.00% 

Sunscreen

Uses

Helps prevent sunburn.Higher SPF gives more sun protection.

DIRECTIONS

Shake well before using spray. Spray liberally 15 minutes before sun exposure.

Reapply after 80 minutes of swimming or sweating , after towel drying, at least every 2 hours

Sun Protection Measures.Spending tme 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 shirt, pants, hats, and sunglasses.
children under 6 months: Ask a doctor.

Warnings

For external use only.

Flammable:Dp not use near heat, flame or while smoking

Do not useon damage or broken skin

When using this productkeep out of eyes. Rinse with water to remove.

Do notpunncture or incinerate. Content under pressure.

Do notstore above 120F

Stop use and ask doctor ifrash occurs

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Inactive Ingredeints

Alcohol Denat.
Aloe Barbadensis Leaf Juice
Butyloctyl Salicylate
Inulin
Magnesium Chloride
Oryza Sativa (Rice) Bran Oil
Polyester-8
VA/Butyl Maleate/Isobornyl Acrylate Copolymer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SPF 50 DRY TOUCH CONTINUOUS NO FRAGRANCE 
homosalate 10.00% octisalate 5.00% avobenzone 3.00% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72344-111
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	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)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
INULIN (UNII: JOS53KRJ01)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
ORYZA SATIVA (RICE) BRAN (UNII: R60QEP13IC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72344-111-03	170 g in 1 CAN; Type 0: Not a Combination Product	05/04/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	05/04/2026

Labeler - Surface Products Corp (010777036)

Registrant - Inspec Solutions LLC (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC.		081030372	manufacture(72344-111)