Label: MANGO BAY SPF 50 SPORT- avobenzone, humosalate, octisalate, octocrylene spray
- NDC Code(s): 72667-037-01
- Packager: Inspec Solutions
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 6, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- WHEN USING
- PURPOSE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
INACTIVE INGREDIENT
Behenyl Alcohol
BHT
Butyloctyl Salicylate
Caprylyl Methicone Dimethicone
Dimethyl Capramide
Disodium EDTA
Ethylhexyl Stearate
Ethylhexylglycerin
Fragrance
Glyceryl Stearate Hydrated Silica
PEG-100 Stearate
Phenoxyethanol
Polyester-8
Sodium Polyacrylate
Styrene/Acrylates Copolymer
Trideceth-6
Trimethylsiloxysilicate
VP/Hexadecene Copolymer
Water
Xanthan Gum
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- ASK DOCTOR
-
DOSAGE & ADMINISTRATION
Directions
- Apply liberally to cool, dry skin 15 minutes before sun exposure. Spray 4-6 inches from body, then rub in. Spray the sunscreen generously onto your hands first, and then rub it into the face.
Reapply:
- after 80 minutes of swimming or sweating.
- immediately after towel drying.
- at least every 2 hours
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 of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10am - 2pm.
- wear long-sleeved shirts, pants, hats, and sunglasses.
- Children under 6 months: Ask a doctor.
- OTHER SAFETY INFORMATION
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MANGO BAY SPF 50 SPORT
avobenzone, humosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72667-037 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 15 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL Inactive Ingredients Ingredient Name Strength FRAGRANCE 13576 (UNII: 5EM498GW35) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) ALOE VERA LEAF (UNII: ZY81Z83H0X) BEHENYL BEHENATE (UNII: K8NU647RJ0) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2) ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72667-037-01 177 mL in 1 CAN; Type 0: Not a Combination Product 06/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/25/2022 Labeler - Inspec Solutions (081030372) Establishment Name Address ID/FEI Business Operations Inspec Solutions 081030372 manufacture(72667-037)
