Label: NAELI DAY MOISTURIZER SPF 30- octisalate, octocrylene, avobenzone lotion

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

Drug Label Information

Updated November 5, 2023

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  • DRUG FACTS

  • Active Ingredients

    Octisalate 5.00%

    Octocrylene 5.00%

    Avobenzone 3.00%

    Purpose

    Sunscreen

  • Uses:

    • Helps prevent sunburn.
    • higher SPF gives more sunburn protection
    • If used as directed with other sun protection measures (see ), decreases the risk of skin cancer and early skin aging caused by the sun Directions
  • Warnings:

    For external use only not intended for ingestion.

    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 or irritation develops and lasts.

    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 and as needed.
    • Children under 6 months of age: ask a doctor.
    • Reapply at least every 2 hours
    • Use a water-resistant sunscreen if swimming or sweating
    • Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: Sun Protection Measures.
    • Limit time in the sun, especially from 10 a.m.-2 p.m.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Inactive Ingredients:

    Aqua (Deionized Water), Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Caprylic/Capric Triglyceride, C12-15 Alkyl Benzoate, Cetearyl Alcohol, Cetearyl Glucoside, Saccharide Isomerate, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Argania Spinosa (Argan) Oil, Isostearyl Palmitate, Mangifera Indica (Mango) Butter, Tocopheryl Acetate (Vitamin E), Camellia Sinensis (Green Tea) Extract, Hydrolyzed Oat Protein, Glycerin, Butylene Glycol, Carbomer, Polysorbate 20, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Hyaluronic Acid, Butyrospermum Parkii (Shea) Butter, Hydrolyzed Collagen, Punica Granatum (Pomegranate) Extract, Tetrahexyldecyl Ascorbate (Vitamin C), Centella Asiatica (Gotu Kola) Extract, Retinyl Palmitate (Vitamin A), Theobroma Cacao (Cocoa) Butter, a-Lipoic Acid, Allantoin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium PCA, Ceramide NG, Lavandula Angustifolia (Lavender) Oil, Cocos Nucifera (Coconut) Oil, Sodium Hydroxide, Glyceryl Caprylate, Glyceryl Undecylenate.

  • Other Information:

    • Protect the product in this container from excessive heat and direct sun.
  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    NAELI DAY MOISTURIZER SPF 30 
    octisalate, octocrylene, avobenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73670-049
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE50 mg  in 1 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    SACCHARIDE ISOMERATE (UNII: W8K377W98I)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    LAURETH-7 (UNII: Z95S6G8201)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    ISOSTEARYL PALMITATE (UNII: 9EHU0R7ER1)  
    MANGO (UNII: I629I3NR86)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)  
    PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    POMEGRANATE (UNII: 56687D1Z4D)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    COCOA (UNII: D9108TZ9KG)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    CERAMIDE NG (UNII: C04977SRJ5)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)  
    GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73670-049-001 in 1 CARTON03/10/2020
    140 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/10/2020
    Labeler - Alli LLC (117308980)
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