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Lantiseptic (Summit Industries, Inc.)

Available Formats

Dosage Form Package Information Links
CREAM 14.2 g in 1 PACKET (12090-0016-2) Label Information
CREAM 113 g in 1 TUBE (12090-0016-1) Label Information
CREAM 227 g in 1 JAR (12090-0016-3) Label Information

Complete Lantiseptic Information

  • Drug Facts


  • Active Ingredient

    Lanolin USP 30%

    Purpose

    Skin Protectant


  • Uses

    Helps protect ulcer prone skin. For treatment of cracked skin, minor burns or irritations. Helps prevent chafing and dryness.


  • Warnings

    For external use only. 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. If swallowed, get medical help or contact a Poison Control Center right away.

    Keep out of reach of children.

  • Directions

    Gently cleanse and dry area. Massage liberally into affected area as needed. Cover treated feet.


  • Other Information

    Store at 15-30°C (59-86°F)


  • Inactive Ingredients

    Beeswax (Yellow Wax), Disodium EDTA, DMDM Hydantoin + IPBC, Lanolin Alcohol, Mineral Oil, Petrolatum, Purified Water, Sodium Borate, Sorbitan Sesquioleate.


  • Questions or Comments?

    844-7SANTUS or visit www.lantiseptic.com


  • Package Labeling:

    Dry Skin


  • INGREDIENTS AND APPEARANCE
    LANTISEPTIC DRY SKIN THERAPY 
    lanolin cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:12090-0016
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 300 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    LANOLIN ALCOHOLS (UNII: 884C3FA9HE)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:12090-0016-2 14.2 g in 1 PACKET; Type 0: Not a Combination Product 03/02/2016
    2 NDC:12090-0016-1 113 g in 1 TUBE; Type 0: Not a Combination Product 03/02/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 03/02/2016
    Labeler - Santus LLC (079868223)