LANASHIELD (LANOLIN) OINTMENT [DYNAREX CORPORATION]

  • Home
  • LANASHIELD (LANOLIN) OINTMENT [DYNAREX CORPORATION]

LANASHIELD (LANOLIN) OINTMENT [DYNAREX CORPORATION]
PDF | XML
NDC 67777-410-04
Set ID 94b277dc-6512-4d36-8485-8ea510097428
Category HUMAN OTC DRUG LABEL
Packager Dynarex Corporation
Generic Name
Product Class
Product Number
Application Number PART347
View All Sections
  • Active Ingredient

    Lanolin 50%

  • Purpose

    Skin Protectant

  • Uses

    • Temporarily protects minor • cuts • scrapes • burns
    • Temporarily protects and helps relieve chafed, chapped, or cracked skin and lips
    • Helps prevent and protect from the drying effects of wind and cold weather
  • Warnings

    For External Use Only

    Do Not Use On

    • deep or puncture wounds
    • animal bites
    • serious burns

    When Using This Product

    • do not get into eyes

    Stop Use And Ask A Doctor If

    • condition worsens
    • symptoms last 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

    Apply as needed

  • Other Information

    • Store at room temperature
    • Avoid excessive heat
  • Inactive Ingredients

    Beeswax (White), EDTA, Emulsifying Wax, Lanolin Alcohol, Mineral Oil, Lavender Perfume,Petrolatum, Purified Water, Sodium Borate

  • Labeling

    Lanashield Label

  • INGREDIENTS AND APPEARANCE
    LANASHIELD 
    lanolin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-410
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN50 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WHITE WAX (UNII: 7G1J5DA97F)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    WATER (UNII: 059QF0KO0R)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-410-04113 g in 1 TUBE; Type 0: Not a Combination Product05/23/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34710/12/2014
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
View All Sections

Related Drugs

Search DailyMed Drugs