Label: SUNLIGHT DAILY FACIAL MOISTURIZING SUNSCREEN- sunscreen lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 20, 2020

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  • Active Ingredient

    Zinc Oxide 15%** 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.

    Children under 6 months of age: Ask a doctor.

    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. to 2 p.m.
    • Wear long-sleeved shirts, pants, hats and sunglasses.
    • Re-apply at least every 2 hours.
    • Use a water resistant sunscreen if swimming or sweating.
  • Other Information

    • Protect the product in this container from excessive heat and direct sun.
  • Inactive Ingredients

    Water (Aqua), Glycerin*, Calophyllum inophyllum (Tamanu) Seed Oil*, Propsnediol, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Jojoba Esters, Disteardimonium Hectorite, Polyglyceryl-2 Isostearate, Polyglyceryl-6 Polyricinloeate, Caprylic/capric Triglyceride, Sesamum Indicum (Sesame) Seed Oil*, Polyhydroxystearic Acid, Tocopherol, Citrus Sinsnsis (Sweet Oralge) Peel Oil*, Euterpe Oleracea (Acai) Pulp Powder*, Lycium Chinense (Goji) Fruit*, Rosmarinus Officinalis (Rosemary) Leaf Powder*, Phenethyl Alcohol, Ethylhexylglycerin

    *Certified Organic Ingredients

    **Non-nanoparticle

  • Questions or comments?

    www.crunchi.com

    (888) 831-3133

  • PRINCIPAL DISPLAY PANEL

    Package Label

  • INGREDIENTS AND APPEARANCE
    SUNLIGHT DAILY FACIAL MOISTURIZING SUNSCREEN 
    sunscreen lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72444-0130
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE4.5 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72444-0130-130 mL in 1 BOX; Type 0: Not a Combination Product07/19/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35207/19/2018
    Labeler - Crunchi LLC (045658615)
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