Label: POOLBAR I SCREAM FOR SUNSCREEN SPF 50 COCONUT AND VANILLA- avobenzone, octisalate, octocrylene liquid
- NDC Code(s): 84953-874-00
- Packager: POOLBAR
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 6, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Use
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Warnings
For external use only
When using this product
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keep out of eyes. Rinse with water to remove.
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Do not puncture or incinerate. Contents under pressure. Do not store it at temperatures above 120ºF.
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Directions
apply liberally 15 minutes before sun exposure
- children under 6 months of age: Ask a doctor.
- Reapply:
- after 80 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- Shake well before use
- hold container 4 to 6 inches from the skin
- spray liberally and rub into the skin by hand
- Do not spray directly on face. spray into hands and apply to face.
- Allow 15 minutes before sun exposure
- Use in well-ventilated area.
- Sun protection measures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with 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
- Inactive ingredients
- Package Labeling:
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INGREDIENTS AND APPEARANCE
POOLBAR I SCREAM FOR SUNSCREEN SPF 50 COCONUT AND VANILLA
avobenzone, octisalate, octocrylene liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84953-874 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 mL OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ALOE VERA LEAF (UNII: ZY81Z83H0X) ASCORBYL PALMITATE (UNII: QN83US2B0N) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CHAMOMILE (UNII: FGL3685T2X) CUCUMBER (UNII: YY7C30VXJT) COCONUT OIL (UNII: Q9L0O73W7L) SUNFLOWER OIL (UNII: 3W1JG795YI) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84953-874-00 150 mL in 1 CAN; Type 0: Not a Combination Product 07/25/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/25/2025 Labeler - POOLBAR (119319250) Registrant - Pure Source, LLC (080354456)
