Label: DAILY FACIAL MOISTURIZER SPF 25- sunscreen cream

  • NDC Code(s): 0096-0721-07, 0096-0721-45
  • Packager: Person and Covey
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 27, 2024

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  • Uses

    -Moisturizes and helps to relieve irritated and sensitive skin

    -Higher SPF gives more sunburn protection

    -Water resistant

  • Keep Out of the Reach of Children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Warnings

    For external use only

  • .Stop Use

    Stop Use and ask a Doctor if a rash rash or irritation develops and lasts

  • Questions

    Questions? Please call 1 (800) 423-2341

  • Inactive Ingredients

    Purified Water, Propylene Glycol Dioctanoate, Petrolatum, Glycerin, Glyceryl Stearate, PEG-100 Stearate, DEA-Cetyl Phosphate, Stearic Acid, Hyaluronic Acid, Benzyl Alcohol, Dimethicone, Cyclomethicone, PVP/Eicosene Copolymer, Silica, Sodium Carbomer 941, Allantoin, Disodium EDTA, Magnesium Aluminum Silicate

  • Other Information

    -High sun protection product

    -Sun Alert: limiting sun exposure, wearing sun protective clothing and using sunscreens may reduce the risk of skin aging, skin cancer and other harmful effects of the sun.

    -Avoid exposure to extreme heat or cold.

  • Active Ingredients

    Octinoxate......7.5% Sunscreen

    Homosalate....6.0% Sunscreen

    Avobenzone...3.0% Sunscreen

    Octocrylene....1.5% Sunscreen

  • Directions

    -Apply DML Daily Facial Moisturizer liberally and evenly 15-20 minutes before sun exposure and message in gently, allowing it to dry. Reapply as needed or as directed by your Dermatologist.

    -DML Daily Facial is an excellant make-up base.

  • Purpose

    Sunscreen

  • Package Label Principal Display Panel

    DML Facial Moisturier

  • INGREDIENTS AND APPEARANCE
    DAILY FACIAL MOISTURIZER  SPF 25
    sunscreen cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0096-0721
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE0.06 g  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE0.03 g  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.075 g  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.015 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE 1000 (UNII: MCU2324216)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0096-0721-077 g in 1 BOTTLE; Type 0: Not a Combination Product08/01/1991
    2NDC:0096-0721-4545 g in 1 BOTTLE; Type 0: Not a Combination Product08/01/1991
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/01/1991
    Labeler - Person and Covey (008482473)
    Establishment
    NameAddressID/FEIBusiness Operations
    Person and Covey008482473manufacture(0096-0721)
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