Dollar General Studio Selection Sun Sunscreen Lotion Broad Spectrum SPF 70

Dollar General Studio Selection Sun Sunscreen Broad Spectrum SPF 70 by

Drug Labeling and Warnings

Dollar General Studio Selection Sun Sunscreen Broad Spectrum SPF 70 by is a Otc medication manufactured, distributed, or labeled by Dolgencorp, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOLLAR GENERAL STUDIO SELECTION SUN SUNSCREEN BROAD SPECTRUM SPF 70- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion 
Dolgencorp, LLC

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Dollar General Studio Selection Sun Sunscreen Lotion Broad Spectrum SPF 70

Active ingredients

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%, Octocrylene 10.0%, Oxybenzone 6.0%

Purpose

Sunscreen

Uses

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

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 ask doctor if​

• rash occurs.

​Keep out of reach of children. ​If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply liberally 15 minutes before sun exposure

reapply:
after 80 minutes of swimming or sweating
immediately after towel drying
at least every 2 hours

children under 6 months: Ask a doctor

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

Other information

protect the product in this container from excessive heat and direct sun
may stain or damage some fabrics, materials or surfaces

Inactive ingredients

Water, Butylene Glycol, Microcrystalline Cellulose, Glyceryl Stearate, Behenyl Alcohol, Benzyl Alcohol, Diethylhexyl Syringylidenemalonate, Tocopherol (Vitamin E), Retinyl Palmitate (Vitamin A palmitate), Sodium Ascorbyl Phosphate, Stearic Acid, Palmitic Acid, Lauryl Alcohol, Myristyl Alcohol, Cetyl Alcohol, Lecithin, Caprylic/Capric Triglyceride, Chlorphensin, Cellulose Gum, Butylated PVP, Disodium EDTA

DOLLAR GENERAL STUDIO SELECTION SUN SUNSCREEN BROAD SPECTRUM SPF 70 
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55910-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	50 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	150 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	30 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	60 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
DOCOSANOL (UNII: 9G1OE216XY)
BENZYL ALCOHOL (UNII: LKG8494WBH)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
STEARIC ACID (UNII: 4ELV7Z65AP)
PALMITIC ACID (UNII: 2V16EO95H1)
LAURYL ALCOHOL (UNII: 178A96NLP2)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
CETYL ALCOHOL (UNII: 936JST6JCN)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
CHLORPHENESIN (UNII: I670DAL4SZ)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55910-036-11	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/26/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/26/2015	12/07/2024

Labeler - Dolgencorp, LLC (068331990)

Revised: 10/2024

Document Id: 24b24fe9-a67d-6eb1-e063-6394a90aa23f

34390-5

Set id: c709045c-5f55-e4f4-e053-2995a90ad6b9

Version: 2

Effective Time: 20241017