Label: GOOD TIMES SPF 50 SUNSCREEN- homosalate, octocrylene, octisalate, avobenzone spray
- NDC Code(s): 72098-009-01
- Packager: EVERYDAY GROUP LIMITED
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2023
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Directions
Shake well. Hold container 4 to 6 inches from skin to apply. • Apply liberally 15 minutes before sun exposure • • Spray on hands then apply to face. • Do not apply in windy conditions. • Use in well-ventilated area. • Reapply: • After 80 minutes of swimming or sweating • Immediately after towel drying • At least every 2 hours • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the 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. to 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months of age: Ask a doctor Do not spray directly into face.Sun Protection Measures:
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INGREDIENTS AND APPEARANCE
GOOD TIMES SPF 50 SUNSCREEN
homosalate, octocrylene, octisalate, avobenzone sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72098-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DIBUTYL MALEATE (UNII: 4X371TMK9K) PAPAYA SEED OIL (UNII: N4P40Z2DDB) SUNFLOWER OIL (UNII: 3W1JG795YI) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72098-009-01 150 mL in 1 CAN; Type 0: Not a Combination Product 06/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2023 Labeler - EVERYDAY GROUP LIMITED (664624682)
