Solar Sense SPF-50 Daily Facial Sunscreen

Solar Sense SPF 50 Daily Facial Sunscreen by

Drug Labeling and Warnings

Solar Sense SPF 50 Daily Facial Sunscreen by is a Otc medication manufactured, distributed, or labeled by CCA Industries, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SOLAR SENSE SPF 50 DAILY FACIAL SUNSCREEN- homosalate, octocrylene, octisalate, avobenzone cream 
CCA Industries, Inc

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Solar Sense SPF-50 Daily Facial Sunscreen

Drug Facts

Active Ingredients

Homosalate 10.0%

Octocrylene 10.0%

Octisalate 5.0%

Avobenzone 3.0%

Purpose

Sunscreen

Uses

Helps prevent sunburn

If used as directed with other sun protection measure (see directions), decreases the risk of skin cancer and early skin aging caused by the sun

Higher SPF gives more sunburn protection.

Warnings

For external use only.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use and consult physician if

irritation or rash developes and lasts.

Keep out of reach of children.

If product is swallowed, get medical attention or contact poison control center immediately.

Directions

Apply liberally 15-minutes before sun exposure

At least every two-hours immediately after swimming, sweating or towel drying   REAPPLY:

Children under 6 months of age: ask a doctor.

Spending time in the sun increases your risk of skin cancer and  early skin aging. To decrease this risk, SUN PROTECTION MEASURES:

regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including:

Limit time in the sun, especially between 10am - 2pm

Wear long sleeve shirts, pants, hats and sunglasses.

Inactive Ingredients

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Butyrospermum Parkii (Shea) Butter, Camellia Sinensis (Green Tea) Extract, Cetearyl Alcohol, Cetearyl Olivate, Cocamidopropyl Betaine, Cucumis Sativus (Cucumber) Extract, Cyclopentasiloxane, Cyclotetrasiloxane, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, C13-14 Isoparaffin, Isopropyl Myristate, Laureth-7, Parfum (Fragrance), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate-20, Punica Granatum (Pomegranate) Extract, Sorbitan Olivate, Tocopheryl Acetate (Vitamin E), Zemea (Corn) Propanediol.

Other information

Protect this product from excessive heat and direct sunlight.

Questions?

Call 1-800-595-6230 or visit www.solarsensespf.com

Package Labeling:

SOLAR SENSE SPF 50 DAILY FACIAL SUNSCREEN 
homosalate, octocrylene, octisalate, avobenzone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61543-0154
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	100 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
SHEA BUTTER (UNII: K49155WL9Y)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CUCUMBER SEED (UNII: BT3S9L53JK)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 4 (UNII: CZ227117JE)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
SUNFLOWER OIL (UNII: 3W1JG795YI)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
LAURETH-7 (UNII: Z95S6G8201)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
SORBITAN OLIVATE (UNII: MDL271E3GR)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CORN (UNII: 0N8672707O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61543-0154-1	1 in 1 CARTON	07/08/2020	06/01/2023
1		50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/08/2020	06/01/2023

Labeler - CCA Industries, Inc (106771041)

Revised: 10/2024

Document Id: 25472b6f-892c-cd8a-e063-6394a90a72b9

34390-5

Set id: e067e7ca-1b84-44ce-8f17-2883f7a715b4

Version: 4

Effective Time: 20241025