Label: NIVEA MEN MAXIMUM HYDRATION FACE- avobenzone, octisalate, octocrylene lotion

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

Drug Label Information

Updated April 10, 2024

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

  • ACTIVE INGREDIENT

    Active ingredients

    Avobenzone 3%

    Octisalate 4.7%

    Octocrylene 8.4%

  • PURPOSE

    Purpose

    Sunscreen

  • INDICATIONS & USAGE

    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

    Warnings

    For external use only

  • DO NOT USE

    Do not use on damaged or broken skin

  • WHEN USING

    When using this product keep out of eyes.

    Rinse with water to remove.

  • STOP USE

    Stop use and ask a doctor if rash occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed,

    get medical help or contact a Poison Control

    Center right away.

  • QUESTIONS

    Questions or comments?

    1-800-227-4703

  • DOSAGE & ADMINISTRATION

    Directions

    For sunscreen use:

    • apply liberally 15 minutes before sun exposure

    • use a water resistant sunscreen if swimming or sweating

    • reapply at least every 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 of age: Ask a doctor

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Water, Isopropyl Palmitate, Glycerin, Alcohol Denat.,

    Tapioca Starch, Cetearyl Alcohol, Glyceryl

    Stearate Citrate, Aloe Barbadensis Leaf Juice

    Powder, Panthenol, Tocopheryl Acetate,

    Phenoxyethanol, 1,2-Hexanediol,

    Carbomer, Fragrance, Ethylhexylglycerin,

    Acrylates/C10-30 Alkyl Acrylate

    Crosspolymer, Pantolactone, Citric Acid, Sodium Hydroxide,

    Trisodium EDTA.

  • PRINCIPAL DISPLAY PANEL

    NIVEA MEN

    Maximum Hydration Face Lotion

    Broad Spectrum SPF 15
    Sunscreen

    Moisturizes and Protects

    Pro-vitamin B5 and Aloe Vera

    nmenmaxhy

    nmmaxhylotioncarton

  • INGREDIENTS AND APPEARANCE
    NIVEA MEN MAXIMUM HYDRATION FACE 
    avobenzone, octisalate, octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10356-567
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.7 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE8.4 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PANTHENOL (UNII: WV9CM0O67Z)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    EDETATE TRISODIUM (UNII: 420IP921MB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    ALOE (UNII: V5VD430YW9)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PANTOLACTONE (UNII: J288D7O0JS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10356-567-1675 mL in 1 TUBE; Type 0: Not a Combination Product07/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/01/2022
    Labeler - Beiersdorf Inc (001177906)