Label: BLT 2- lidocaine hcl ointment

  • NDC Code(s): 70372-728-01
  • Packager: CENTURA PHARMACEUTICALS INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 15, 2022

If you are a consumer or patient please visit this version.

  • 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 not finalpart34811/21/2016
    Labeler - CENTURA PHARMACEUTICALS INC (084921637)
    Registrant - CENTURA PHARMACEUTICALS INC (084921637)