FDA.reportPublic FDA data

Dollar General Studio Selection Sun Sunscreen Lotion Broad Spectrum SPF 70

Manufacturer
Dolgencorp, LLC
Effective date
2024-10-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:52:02

Label at a glance#

ProductDollar General Studio Selection Sun Sunscreen Broad Spectrum SPF 70
Active ingredientOCTOCRYLENE, OCTISALATE, HOMOSALATE, AVOBENZONE, OXYBENZONE
Label structure12 sections

Indications and 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

Dosage and administration

• 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 su...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

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

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

​For external use only

OTC - DO NOT USE SECTION

​Do not use

  • ​​on damaged or broken skin

OTC - WHEN USING SECTION

​When using this product​ keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

​Stop use and ask doctor if​

  • rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DG77008D1DG77008D1

DG77003DDG77003D

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55910-03655910-036-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01IACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
GLYCERYL 1-STEARATE258491E1RZIACT
DOCOSANOL9G1OE216XYIACT
BENZYL ALCOHOLLKG8494WBHIACT
DIETHYLHEXYL SYRINGYLIDENEMALONATE3V5U97P248IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
STEARIC ACID4ELV7Z65APIACT
PALMITIC ACID2V16EO95H1IACT
LAURYL ALCOHOL178A96NLP2IACT
MYRISTYL ALCOHOLV42034O9PUIACT
CETYL ALCOHOL936JST6JCNIACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311IACT
EGG PHOSPHOLIPIDS1Z74184RGVIACT
CHLORPHENESINI670DAL4SZIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
SODIUM ASCORBYL PHOSPHATE836SJG51DRIACT
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
HOMOSALATEV06SV4M95SACTIB
AVOBENZONEG63QQF2NOXACTIB
OXYBENZONE95OOS7VE0YACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
24b24fe9-a67d-6eb1-e063-6394a90aa23fc709045c-5f55-e4f4-e053-2995a90ad6b92024-10-17WarningsExact identifier
spl id: 24b24fe9-a67d-6eb1-e063-6394a90aa23f
spl set id: c709045c-5f55-e4f4-e053-2995a90ad6b9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.