Label: DOLLAR GENERAL STUDIO SELECTION SUN SUNSCREEN BROAD SPECTRUM SPF 85 WITH ALOE- avobenzone, homosalate, octisalate, octocrylene, oxybenzone aerosol, spray
- NDC Code(s): 55910-008-37
- Packager: Dolgencorp, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 13, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- FLAMMABLE:
- DO NOT USE
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WHEN USING
When using this product • keep out of eyes. Rinse with water to remove. •keep away from face to avoid breathing it. • do not puncture or incinerate. Contents under pressure. • do not store at temperatures above 120° F. Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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Directions
•Spray liberally and spread evenly by hand 15 minutes before sun exposure
•Hold can 4 to 6 inches away from skin to apply
•Do not spray directly into face. Spray into hand then apply to face.
•Use in a well-ventilated area
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
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Inactive ingredients
alcohol denat., isobutane, VA/butyl maleate/isobornyl acrylate copolymer, caprylyl glycol, cyclopentasiloxane, cyclohexasiloxane, fragrance, polyglyceryl-3 stearate/isostearate/dimer dilinoleate crosspolymer, lauryl PEG-8 dimethicone, phenylisopropyl dimethicone, ascorbyl palmitate, methyl dihydroabietate, tocopheryl acetate, mineral oil, panthenol, water, aloe barbadensis leaf juice
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DOLLAR GENERAL STUDIO SELECTION SUN SUNSCREEN BROAD SPECTRUM SPF 85 WITH ALOE
avobenzone, homosalate, octisalate, octocrylene, oxybenzone aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-008 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg in 1 g 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 OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 g Inactive Ingredients Ingredient Name Strength LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ALCOHOL (UNII: 3K9958V90M) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CAPRYLYL GLYCOL (UNII: 00YIU5438U) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTHENOL (UNII: WV9CM0O67Z) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) ASCORBYL PALMITATE (UNII: QN83US2B0N) MINERAL OIL (UNII: T5L8T28FGP) WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) ISOBUTANE (UNII: BXR49TP611) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-008-37 156 g in 1 CAN; Type 0: Not a Combination Product 03/08/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/08/2018 Labeler - Dolgencorp, LLC (068331990)