Label: DAILY BROAD SPECTRUM SERUM SOLARDROPS- zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 5, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredients

    Non-Nano Zinc Oxide 24.5%

  • Purpose

    Sunscreen

  • Uses

    helps prevent sunburn if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • Warnings

    • For external use only

    • Do not use on damaged or broken skin

    • When using this product keep out of eyes. Rinse with water to remove.

    • Stop use and ask a doctor if rash occurs

    • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Apply liberally 15 minutes before sun exposure
    • reapply • after 80 minutes of swimming or sweating • immediately after towel drying • at least ever 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 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 doctor

  • Other Information

    Protect this product from excessive heat and direct sun
    ■ may stain fabrics

  • Inactive Ingredients

    Water (Aqua), C13-15 Alkane, Ethyl Macadamiate, Caprylic/Capric Triglyceride, Polyhydroxystearic Acid, Propanediol, Kaolin, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Polyglyceryl-3 Polyricinoleate, Isostearic Acid, Lecithin, Opuntia Ficus-Indica (Prickly Pear Cactus) Leaf Cell Extract, Balanites Aegyptiaca (Desert Date) Kernel Oil, Hippophae Rhamnoides (Sea Buckthorn) Kernel Extract, Dipteryx Odorata, Lavandula Angustifolia (Lavender) Oil, Origanum Majorana (Sweet Marjoram) Leaf Oil, Pogostemon Cablin (Patchouli) Oil, Polycitronellol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Polyquaternium-90, Bentonite, Sodium Chloride, Squalane, Triethyl Citrate, Phenoxyethanol, Ethylhexylglycerin, Iron Oxides (CI 77491, CI 77492)

  • Questions?

    E-mail hello@onekind.us or call 323-275-9380

  • PRINCIPAL DISPLAY PANEL

    25X110 SolardropsSPF-A TubeOnekind Solardrops Carton-v2-outlined (1)

  • INGREDIENTS AND APPEARANCE
    DAILY BROAD SPECTRUM SERUM SOLARDROPS 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83260-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE245 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    KAOLIN (UNII: 24H4NWX5CO)  
    POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)  
    HIPPOPHAE RHAMNOIDES SEED (UNII: ZD5PJT4UZF)  
    C13-15 ALKANE (UNII: 114P5I43UJ)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    BENTONITE (UNII: A3N5ZCN45C)  
    ETHYL MACADAMIATE (UNII: ANA2NCS6V1)  
    SWEET MARJORAM OIL (UNII: ICH7BE016E)  
    POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)  
    ISOSTEARIC ACID (UNII: X33R8U0062)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    WATER (UNII: 059QF0KO0R)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    SQUALANE (UNII: GW89575KF9)  
    OPUNTIA FICUS-INDICA LEAF (UNII: 5VM709H93V)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)  
    DIPTERYX ODORATA SEED (UNII: D43A5L1U6L)  
    DESERT DATE (UNII: IDC07J5J5Q)  
    POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83260-100-0128 g in 1 TUBE; Type 0: Not a Combination Product12/05/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/05/2023
    Labeler - Motley Brands LLC (071571407)