BROAD SPECTRUM SUNSCREEN SPF 30- avobenzone, homosalate, octisalate spray

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 OLD EAST MAIN CO., Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3%

Homosalate 10%

Octisalate 5%

Purpose

Sunscreen

Uses

• helps prevent sunburn
• if used as directed with other sun protections measures (see Directions), decreases the rist of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Flammable:

Keep away from fire or flame.

• after application, wait until product dries before approaching a source of heat or flame, or before smoking

Do not use

• on damaged or broken skin

When using this product

• keep out of eyes. Rinse with water to remove.
• contents under pressure. Do not punture or incinerate. Do not store at temperature above 120°F.

Stop use and ask a doctor if

• rash occurs

Keep out of reach of children.

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

Directions

• spray liberally and spread evenly by hand 15 minutes before sun exposure
• apply to all skin exposed to the sun
• hold container 4 to 6 inches from the skin to apply
• do not spray directly into face. Spray on hands then apply to face.
• do not apply in windy conditions
• use in a well-ventilated area and avoid inhalation
• 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 value of 15 or higher and other sun protection measures including:
• limit time in the sun, especially from 10 a.m.–2 p.m.
• wear long-sleeved shirts, pants, hats and sunglasses
• children under 6 months of age: Ask a doctor

Other information

• protect the product in this container from excessive heat and direct sun

Inactive ingredients

alcohol denat., diethylhexyl 2,6-naphthalate, acrylates/octylacrylamide copolymer, diisopropyl adipate, neopentyl glycol diheptanoate, butyloctyl salicylate, fragrance, tocopheryl acetate

Disclaimer

May stain or damage some fabrics or surfaces

OCTINOXATE FREE, OXYBENZOE FREE

*This product is not manufactured or distributed by Sun Bum LLC, distributor of Sun Bum® Premium Moisturizing Sunscreen Spray Broad Spectrum SPF 30.

Adverse Reaction

Distirubted by OLD EAST MAIN CO.

100 Mission Ridge 

Goodlettesville, TN 37072

Principal Panel Display

Studio Selection ® Sun

SUNSCREEN SPRAY

BROAD SPECTRUM SOF

Compare to Sun Bum ®Sunscreen Spray Broad Spectrum SPF*

SPF30

Dermatologist Tested

Hypoallergenic

Water Resistant (80 min)

Banana Scent

NEW WT. 5.5OZ (156g)

INGREDIENTS AND APPEARANCE

BROAD SPECTRUM SUNSCREEN SPF 30 
avobenzone, homosalate, octisalate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75712-948
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV)
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75712-948-14	156 g in 1 CAN; Type 0: Not a Combination Product	07/15/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	07/15/2024

Labeler - OLD EAST MAIN CO. (006946172)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(75712-948)