Label: LUMIN BROAD SPECTRUM MOISTURIZER WITH SPF 30 PA HIGH UVA/UVB PROTECTION- zinc oxide cream

  • NDC Code(s): 81234-809-00, 81234-809-02
  • Packager: Pangaea Holdings Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated January 19, 2024

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

  • INGREDIENTS

    Water/Aqua/Eau, Coco-Caprylate, Dicaprylyl Carbonate, Microcrystalline Cellulose, Glycerin, Cetyl Alcohol, Lauryl Glucoside, Capryloyl Glycerin/Sebacic Acid Copolymer, Propanediol, Diheptyl Succinate, Cellulose Gum, Polyglyceryl-2 Dipolyhydroxystearate, Phytic Acid, Simmondsia Chinensis (Jojoba) Seed Oil*, Helianthus Annuus (Sunflower) Seed Oil*, Rosmarinus Officinalis (Rosemary) Leaf Extract, Carica Papaya (Papaya) Fruit Extract, Haematococcus Pluvialis Extract (Astaxanthin), Palmitoyl Tripeptide-38, Caprylhydroxamic Acid, Xanthan Gum, Polyhydroxystearic Acid, Hydroxypropyl Cyclodextrin, Hexanediol, Triethoxycaprylylsilane
    *Certified Organic Ingredients

  • Active Ingredients

    Zinc Oxide 20%

    Purpose

    Sunscreen

  • Warnings

    For external use only. 

    Do not

    apply to damaged or broken skin. Discontinue use if irritation occurs. Over-exposure to the sun is a serious health threat. Do not stay too long in the sun, even while using a sunscreen product.

    Keep babies and young children out of direct sunlight.

  • Directions

    Apply the sunscreen product before sun exposure. Re-apply frequently to maintain protection, especially after perspiring, swimming, or towelling.
    AM: Start with a clean, dry face  and gently rub an almond-sized amount all over the face.
    PM: Wash off with a gentle  cleanser and lukewarm water.

  • Package Labeling:81234-809-00

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  • Package Labeling:81234-809-02

    Label6Label7

  • INGREDIENTS AND APPEARANCE
    LUMIN BROAD SPECTRUM MOISTURIZER WITH SPF 30 PA HIGH UVA/UVB PROTECTION 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81234-809
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION200 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYPROPYL BETADEX (UNII: 1I96OHX6EK)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    WATER (UNII: 059QF0KO0R)  
    COCO-CAPRYLATE (UNII: 4828G836N6)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    FYTIC ACID (UNII: 7IGF0S7R8I)  
    JOJOBA OIL (UNII: 724GKU717M)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ROSEMARY (UNII: IJ67X351P9)  
    PAPAYA (UNII: KU94FIY6JB)  
    HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)  
    PALMITOYL LYSYLDIOXYMETHIONYLLYSINE (UNII: T7A529FB8O)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HEXANEDIOL (UNII: ZIA319275I)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81234-809-001 in 1 BOX01/01/202201/05/2025
    115 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    2NDC:81234-809-021 in 1 BOX01/01/202201/05/2025
    240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only01/01/202201/05/2025
    Labeler - Pangaea Holdings Inc. (081181313)