LANOLIN OINTMENT [DYNAREX CORPORATION]

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LANOLIN OINTMENT [DYNAREX CORPORATION]
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NDC 67777-232-01, 67777-232-02, 67777-232-03, 67777-232-04, 67777-232-05, 67777-232-06
Set ID 87216888-1753-4fd5-a8e0-d8347948b082
Category HUMAN OTC DRUG LABEL
Packager Dynarex Corporation
Generic Name
Product Class
Product Number
Application Number PART347
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  • ACTIVE INGREDIENT

    Active ingredient               Purpose
    Lanolin USP 50%                    Skin Protectant

  • Purpose:

    • Helps prevent and treat diaper dermatitis
    • Protects chafed skin or minor skin irritations due to incontinence and helps seal out wetness
  • Warnings

    For External Use Only

  • Keep Out Of Reach Of Children

    KEEP OUT OF REACH OF CHILDREN

    • If swallowed, get medical help or contact a Poison Control Center right away
  • Indications & Usage

    • Avoid contact with eyes
    • Do not apply to deep or puncture wounds
    • If condition worsens, or does not improve within 7 days, consult a doctor
  • Dosage & Administration

    • Gently cleanse and dry area
    • Apply liberally to affected area as needed
  • Other information:

    • Store at room temperature 20 deg C to 25 deg C 68 deg F to 77 deg F
  • Inactive Ingredients

    Beeswax (Yellow Wax), Fragrance, HEEDTA, Lanolin alcohol, Mineral oil, Oxyguinoline, Petrolatum, Purified water, Sodium borate, Sorbitan sesquioleate

  • Principal Display Panel

    LanolinEnter section text here

  • INGREDIENTS AND APPEARANCE
    LANOLIN 
    lanolin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-232
    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
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    OXYQUINOLINE (UNII: 5UTX5635HP)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-232-012 in 1 CASE
    1144 in 1 BOX
    15 g in 1 PACKET
    2NDC:67777-232-024 in 1 CASE
    236 in 1 BOX
    215 g in 1 PACKET
    3NDC:67777-232-0336 in 1 CASE
    371 g in 1 JAR
    4NDC:67777-232-0424 in 1 CASE
    4113 g in 1 TUBE
    5NDC:67777-232-0524 in 1 CASE
    5127.5 g in 1 JAR
    6NDC:67777-232-0612 in 1 CASE
    6396.8 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34705/12/2010
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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