Label: GREEN DEFENSE DAILY MINERAL SUNSCREEN BROAD SPECTRUM SPF 30- zinc oxide lotion
- NDC Code(s): 72830-265-50
- Packager: Farmacy Beauty LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 28, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- ACTIVE INGREDIENT
- Uses
- Warnings
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Directions
• Apply liberally 15 minutes before sun exposure • Use a water resistant sunscreen if swimming or sweating • Reapply at least every 2 hours
• Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease 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 • Children under 6 months: Ask a doctor Sun Protection Measures.
- Other information
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Inactive ingredients
Water/Aqua/Eau, Caprylic/Capric Triglyceride, C13-15 Alkane, Pentylene Glycol, C15-19 Alkane, Propanediol, Moringa Oleifera Leaf Water, Bis-diglyceryl Polyacyladipate-2, Gluconolactone, Moringa Oleifera Seed Extract, Polyacrylate Crosspolymer-6, Physalis Alkekengi Calyx Extract, Cetearyl Alcohol, Beta-carotene, Inositol, Sodium Dilauramidoglutamide Lysine, Isostearic Acid, Polyhydroxystearic Acid, Lecithin, Polyglyceryl-3 Polyricinoleate, Coco-glucoside, Polyglycerin-3, Tocopherol, Bisabolol, Polyglyceryl-3 Lactate/Laurate, Xanthan Gum, Sodium Citrate, Sclerotium Gum, Arachidyl Glucoside, Citric Acid, Sodium Benzoate, Behenyl Alcohol, Sodium Phytate, Maltodextrin, T-butyl Alcohol, Arachidyl Alcohol, Glucose, Calcium Gluconate
- Package Labeling:
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INGREDIENTS AND APPEARANCE
GREEN DEFENSE DAILY MINERAL SUNSCREEN BROAD SPECTRUM SPF 30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72830-265 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 182.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) C13-15 ALKANE (UNII: 114P5I43UJ) PENTYLENE GLYCOL (UNII: 50C1307PZG) C15-19 ALKANE (UNII: CI87N1IM01) PROPANEDIOL (UNII: 5965N8W85T) MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B) BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T) GLUCONOLACTONE (UNII: WQ29KQ9POT) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) PHYSALIS ALKEKENGI CALYX (UNII: AL7F9NO9HR) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BETA CAROTENE (UNII: 01YAE03M7J) INOSITOL (UNII: 4L6452S749) SODIUM DILAURAMIDOGLUTAMIDE LYSINE (UNII: MNJ7VPT2R5) ISOSTEARIC ACID (UNII: X33R8U0062) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) COCO GLUCOSIDE (UNII: ICS790225B) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) TOCOPHEROL (UNII: R0ZB2556P8) LEVOMENOL (UNII: 24WE03BX2T) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM CITRATE (UNII: 1Q73Q2JULR) BETASIZOFIRAN (UNII: 2X51AD1X3T) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) DOCOSANOL (UNII: 9G1OE216XY) PHYTATE SODIUM (UNII: 88496G1ERL) MALTODEXTRIN (UNII: 7CVR7L4A2D) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) CALCIUM GLUCONATE (UNII: SQE6VB453K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72830-265-50 50 mL in 1 TUBE; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/01/2021 Labeler - Farmacy Beauty LLC (081343430)
