Label: TIEGE HANLEY AM MORNING FACIAL MOISTURIZER WITH SPF 20- avobenzene, octinoxate, octocrylene lotion

  • NDC Code(s): 71714-001-22, 71714-001-75
  • Packager: TIEGE HANLEY, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 13, 2024

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  • ACTIVE INGREDIENT

    Active Ingredients
    Avobenzene 2.5%
    Octinoxate 5.5%
    Octocrylene 2.0%

  • PURPOSE

    SUNSCREEN

  • KEEP OUT OF REACH OF CHILDREN

    ■ If swallowed, get medical help or contact a Poison Control Center right away
    ■ Keep out of reach of children

  • WARNINGS

    Warnings
    ■ For External Use Only
    ■ Do not use on damaged or broken skin
    ■ Stop use and ask a doctor if rash occurs
    ■ When using this product, keep out of eyes
    ■ Rinse with water to remove
    ■ If swallowed, get medical help or contact a Poison Control Center right away
    ■ Keep out of reach of children

  • DOSAGE & ADMINISTRATION

    Directions
    ■ After washing your face, massage a pea-sized
    amount into entire face and neck in a gentle circular motion
    ■ Before sun exposure, use a broad-spectrum sunscreen of SPF
    15 or higher
    ■ Reapply sunscreen at least every two hours
    ■ Use a water-resistant sunscreen if swimming or sweating
    ■ For children under 6 months, ask a doctor

  • INDICATIONS & USAGE

    Uses ■ Helps prevent sunburn

  • INACTIVE INGREDIENT

    Water

    Isodecyl Neopentanoate

    Cyclopentasiloxane

    Bis-PEG-12 Dimethicone Beeswax

    Glycerin

    Glyceryl Stearate

    PEG-100 Stearate

    Phenoxyethanol

    Hydroxypropyl Starch Phosphate

    C18-38 Alkyl Hydroxystearoyl Stearate

    Caprylyl Glycol

    Carbomer

    Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer

    Isohexadecane

    Lavandula Angustifolia (Lavender) Oil

    Rosmarinus Officinalis (Rosemary) Leaf Oil

    Sodium Hydroxide

    Polysorbate 80

    Calendula Officinalis Flower Extract

    Plantago Major Leaf Extract

    Disodium EDTA

  • Tiege Hanley AM Morning Facial Moisturizer with SPF 20 - 0.75 FL. OZ. / 22mL

    Tiege Hanley AM Morning Facial Moisturizer

  • Tiege Hanley AM Morning Facial Moisturizer with SPF 20 - 2.5 FL. OZ. / 75mL

    Tiege Hanley AM Morning Facial Moisturizer

  • INGREDIENTS AND APPEARANCE
    TIEGE HANLEY AM MORNING FACIAL MOISTURIZER WITH SPF 20 
    avobenzene, octinoxate, octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71714-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE25 mg  in 1 mL
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE55 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    BIS-PEG-12 DIMETHICONE (70 MPA.S) (UNII: 2JDK5W22H4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)  
    PLANTAGO MAJOR LEAF (UNII: 7DC28K241X)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)  
    HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) (UNII: 9M44R3409A)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    TETRADECYLOCTADECYL STEARATE (UNII: VX3T5G31XA)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71714-001-2222 mL in 1 TUBE; Type 0: Not a Combination Product09/30/2017
    2NDC:71714-001-7575 mL in 1 TUBE; Type 0: Not a Combination Product09/30/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02009/30/2017
    Labeler - TIEGE HANLEY, Inc (080305325)
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