Label: LBRI PURE N NATURAL SPF 30- zinc oxide cream

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

Drug Label Information

Updated November 5, 2023

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

  • Drug Facts

  • Active ingredients

    Zinc Oxide 19%

    Purpose

    Sunscreen

  • 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

    For external use only.

    Do not use

    on damaged or broken skin.

    When using this product 

    keep out of eyes. Rinse with water to remove.

    Stop use and consult physician

    if irritation or rash develops.

    Keep out of reach of children.

    If product is swallowed, get medical attention or contact poison control center immediately.

  • Directions

    • Apply liberally 15-minutes before sun exposure.
    • Reapply:

    -at least every two-hours.

    -Immediately after swimming, sweating or towel drying.

    Spending time in the sun increases your risk of skin cancer and ealy skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: SUN PROTECTION MEASURES:

    -Limit time in the sun, especially between 10am and 2pm.

    -Wear long sleeve shirts, pants, hats and sunglasses.

    -For children under 6-months, consult a physician.

  • Other ingredients

    1,2-Hexanediol, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Beeswax, Caprylic/Capric Triglyceride, Chamomilla Recutita (Chamomile) Extract, Citrus Aurantium Dulcis (Orange) Extract, Citrus Aurantium Dulcis (Orange) Oil, Citrus Medica Limonum (Lemon) Oil, Citrus Reticulata (Tangerine) Extract, Coco-Caprylate, Decylene Glycol, Ethylhexyl Palmitate, Gluconolactone, Glycerin, Hydrogenated Castor Oil, Isopropyl Myristate, Isopropyl Palmitate, Lecithin, Leuconostoc/Radish Root Ferment Filtrate, Lonicera Caprifolium (Honeysuckle) Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Magnesium Sulfate, Mentha Piperita (Peppermint) Oil, Phenoxyethanol, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Populus Tremuloides Bark Extract, Salix Nigra (Willow) Bark Extract, Silica, Sodium Chloride, Stearic Acid.

  • Other Information:

    Protect the product in this container from excessive heat and direct sunlight.

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    LBRI PURE N NATURAL SPF 30 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71238-326
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION190 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ORANGE (UNII: 5EVU04N5QU)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LEMON (UNII: 24RS0A988O)  
    TANGERINE (UNII: KH3E3096OO)  
    COCO-CAPRYLATE (UNII: 4828G836N6)  
    DECYLENE GLYCOL (UNII: S57M60MI88)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
    LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)  
    LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71238-326-00118 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/01/2018
    Labeler - L'BRI HEALTH & BEAUTY (139751148)