Label: WELLCARE SUNSTICK SUNSCREEN STICK- avobenzone, octinoxate, octocrylene, octisalate stick
WELLCARE SUNSTICK LIP BALM- avobenzone, octinoxate, octocrylene, octisalate stick

  • NDC Code(s): 83149-000-00, 83149-001-00
  • Packager: BAMKO, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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  • Drug Facts

  • Active Ingredient

    (Sunscreen Stick) Avobenzone 2.5mg  Octyl Methoxycinnamate 7.5mg  Octocrylene 10mg  OctyI Salicylate 5mg  (Lip Balm) Avobenzone 0. 5mg. Octyl Methoxycinnamate 5mg  Octocrylene 3  OctyI Salicylate 2.2mg 









    Purpose

    Sunscreen

  • Uses

    Helps prevent sunburn.

  • Warnings

    For external use ony.

    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 product is swallowed, get medical help or contact a Poison Control Center righaway.

  • Directions

    • Apply liberally 15 minutes before sunexposure.
    • Use a water resistant sunscreen if swimming or sweating.
    • Reapply at least every 2 hours.
    • Children under 6 months: Ask a doctor
  • Other Information

    Protect this product from excessive heat and direct sunlight.

  • Inactive Ingredients

    Alpha-Tocopherol Acetate, Bis-Diglyceryl Polyacyladipate-2, Coconut Oil, Ethylhexyl Palmitate, Hydrogenated Soybean Oil, Microcrystalline Wax, Polyisobutylene(2300 MW), Olive Oil, Silicon Dioxide, Stevioside, Synthetic Wax (1200 MW).

  • Inactive Ingredients

    Alpha-Tocopherol Acetate, Bis-Diglyceryl Polyacyladipate-2, Coconut Oil, Ethylhexyl Palmitate, Fragrance (3-(3,4-Methylenedioxyphenyl)-2-methylpropanal, Ethyl vanillin, Propylene glycol, Vanillin), Hydrogenated Soybean Oil, Microcrystalline Wax, Olive Oil, Polyisobutylene(2300 MW), Stevioside, Synthetic Wax (1200 MW).

  • Wellcare Sunstick - Lip Balm, 0.14oz/4g (83149-000-00)

    Label

  • Wellcare Sunstick - Sunscreen Stick, 0.07oz/2g (83149-001-00)

    P1L

    P2L

  • INGREDIENTS AND APPEARANCE
    WELLCARE SUNSTICK SUNSCREEN STICK 
    avobenzone, octinoxate, octocrylene, octisalate stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83149-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE25 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    ETHYL VANILLIN (UNII: YC9ST449YJ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    VANILLIN (UNII: CHI530446X)  
    HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K)  
    STEVIOSIDE (UNII: 0YON5MXJ9P)  
    SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83149-001-002 g in 1 TUBE; Type 0: Not a Combination Product12/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/15/2022
    WELLCARE SUNSTICK LIP BALM 
    avobenzone, octinoxate, octocrylene, octisalate stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83149-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE5 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE30 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE22 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)  
    MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
    POLYISOBUTYLENE (2300 MW) (UNII: DSQ2V1DD1K)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEVIOSIDE (UNII: 0YON5MXJ9P)  
    SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83149-000-004 g in 1 TUBE; Type 0: Not a Combination Product12/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/15/2022
    Labeler - BAMKO, LLC (080220012)
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