Label: NEUTROGENA SUN RESCUE AFTER SUN MEDICATED RELIEF (camphor- synthetic gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 12, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Camphor 0.45%

  • Purpose

    External analgesic

  • Use

    temporarily relieves pain and itching associated with sunburn

  • Warnings

    For external use only.

    Flammable: Keep away from fire or flame

    When using this product avoid contact with eyes

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persist for more than 7 days or clear up and occur again within a few days

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

  • Directions

    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor
  • Other information

    • Store at 20° to 25°C (68° to 77°F)
  • Inactive ingredients

    Water, Alcohol Denat., Triethanolamine, Carbomer, EDTA

  • Questions?

    Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    JOHNSON & JOHNSON CONSUMER INC.
    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 85 g Tube Label

    NEW

    Neutrogena®

    DERMATOLOGIST RECOMMENDED BRAND

    NEUTROGENA®

    SUN

    RESCUE

    AFTER SUN

    MEDICATED RELIEF GEL

    CAMPHOR EXTERNAL ANALGESIC

    pain relief for sunburn

    cools, calms and soothes

    skin on contact

    NET WT 3.0 OZ (85 g)

    Ntg001

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA SUN RESCUE AFTER SUN MEDICATED RELIEF 
    camphor (synthetic) gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0721
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)4.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0721-385 g in 1 TUBE; Type 0: Not a Combination Product10/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01710/01/2021
    Labeler - Kenvue Brands LLC (118772437)
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