Label: BLT 2- lidocaine hcl ointment

  • NDC Code(s): 70372-728-01
  • Packager: CENTURA PHARMACEUTICALS INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 4, 2024

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  • ACTIVE INGREDIENT

    Lidocaine HCL 4%

  • PURPOSE

    Topical Anesthetic

  • USES

    For the temporary relief of pain and itching.

  • WARNINGS

    • For external use only.
    • Avoid contact with eyes or mucus membranes.
    • Do not apply to open or damaged skin.
    • If condition worsens or symptoms persist for
    more than seven days, discontinue use and
    consult physician.
    • If pregnant or breast feeding,contact physician
    prior to use.
    • Keep out of reach of children. If swallowed,
    contact Poison Control Center.
    • Do not use if allergic to any ingredient in ointment.
    • Do not use in large quantities, particularly over
    raw surfaces or blistered areas.

  • DIRECTIONS

    Adults and children two-years of age or
    older: Apply to affected area not more than three to
    four times daily. Children under two-years of age:
    consult a physician.

  • OTHER INFORMATION

    Store below 77° F (25° C). Avoid
    direct sunlight.

  • INACTIVE INGREDIENTS

    Acrylates, C10-30 Alkyl Acrylate Crosspolymer, Aqua (Deionized Water), Beeswax, Benzyl Alcohol, Cetyl Alcohol, Dehydroacetic Acid, Glycerin, Helianthus Anuus (Sunflower) Oil, Polysorbate 20, Sodium Hydroxide, Stearic Acid.

  • KEEP OUT OF REACH OF CHILDREN

  • PACKAGE LABELING

    BLT 2

  • INGREDIENTS AND APPEARANCE
    BLT 2 
    lidocaine hcl ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70372-728
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70372-728-015 g in 1 POUCH; Type 0: Not a Combination Product11/21/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/21/2016
    Labeler - CENTURA PHARMACEUTICALS INC (084921637)
    Registrant - CENTURA PHARMACEUTICALS INC (084921637)
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