NUGLOW (AVOBENZONE, OCTINOXATE, AND ZINC OXIDE) CREAM [G.S. COSMECEUTICAL USA, INC.]

NUGLOW (AVOBENZONE, OCTINOXATE, AND ZINC OXIDE) CREAM [G.S. COSMECEUTICAL USA, INC.]
PDF | XML

NDC 65113-8503-3
Set ID 5636a6e4-0747-41a6-9308-fd734784a2e2
Category HUMAN OTC DRUG LABEL
Packager G.S. COSMECEUTICAL USA, INC.
Generic Name
Product Class
Product Number
Application Number PART352
  • DIRECTIONS

    After cleansing, apply liberally to face daily. Apply evenly before sun exposure. Reapply as needed after towel drying, swimming or perspiring.

    Children under 6 months: ask a doctor.

  • WARNINGS

    For external use only.

    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.

  • QUESTIONS?

    1-866-605-9510 or visit www.nuglowskincare.com.

  • PURPOSE

    Daytime Therapy With SPF15

  • ACTIVE INGREDIENTS

    Avobenzone 1.0%, Octinoxate 7.0%, Zinc Oxide 4.0%.

  • INACTIVE INGREDIENTS

    Aqua (Water), Caprylic/Capric Triglyceride, Glyceryl Stearate SE, Butyrospermum Parkii (Shea Butter), Polysorbate 60, Cetyl Alcohol, Dimethicone, Cetyl Ricinoleate, Stearyl Alcohol, Persea Gratissima (Avocado) Oil, Glycerin, Sodium Hyaluronate, Camellia Oleifera (Green Tea) Leaf Extract, Chrondrus Crispus (Carrageenan), Sodium PCA, Xanthan Gum, Tocopheryl Acetate, Ascorbic Acid, Lactic Acid, Glucose, Triethoxycaprylylsilane, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol.

  • SPL UNCLASSIFIED SECTION

    For expiration date, see bottom of jar.

    Made in the U.S.A. for NuGlow, Los Angeles, CA 90049

    Reorder# 70825
    Rev 8/10

  • PRINCIPAL DISPLAY PANEL - 34g Jar Label

    NuGlow®

    Daytime Therapy
    With SPF15

    Net Weight 1.2 Oz./34g e

    PRINCIPAL DISPLAY PANEL - 34g Jar Label
  • INGREDIENTS AND APPEARANCE
    NUGLOW   DAYTIME THERAPY WITH SPF 15
    avobenzone, octinoxate, and zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65113-8503
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1 g  in 100 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    AVOCADO OIL (UNII: 6VNO72PFC1)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65113-8503-334 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart35210/15/2010
    Labeler - G.S. COSMECEUTICAL USA, INC. (017014734)
    Establishment
    NameAddressID/FEIBusiness Operations
    G.S. COSMECEUTICAL USA, INC.017014734MANUFACTURE

Related Drugs