Label: BACTINE MAX ANTIBIOTIC AND LIDOCAINE MAX PAIN RELIEF- lidocaine ointment

  • NDC Code(s): 65197-827-05
  • Packager: WellSpring Pharmaceutical Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 8, 2023

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

View All Sections
  • Active Ingredients (w/w)

    Lidocaine (40 mg)
    Bacitracin Zinc (500 units)
    Polymyxin B Sulfate (10,000 units)

  • Purpose 

    External analgesic
    First aid antibiotic
    First aid antibiotic

  • Uses

    First aid to help prevent infection in and temporarily relieves pain due to

    • minor cuts
    • scrapes
    • burns
  • Warnings

    For external use only

    Allergy alert

    • do not use If you are allergic to any of the ingredients

    Do not use

    • in or near the eyes
    • on large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    When using this product

    • do not use longer than 1 week unless directed by a doctor

    Stop use and ask a doctor if

    • condition lasts or gets worse
    • symptoms last for more than 7 days or clear up and come back within a few days
    • a rash or other allergic reaction occurs

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center immediately.
  • Directions

    Adults and children 2 years and older:

    • clean affected area
    • apply a small amount (equal to the surface area of tip of finger) on area 1 to 3 times daily.
    • may be covered with a sterile bandage.

    Children under 2 years: ask a doctor

  • Other information

    Store at controlled room temperature 68º-77ºF (20º-25ºC).

  • Inactive ingredients

    Gossypium Herbaceum (Cotton) Seed Oil, Olea Europaea (Olive) Fruit Oil, Petrolatum, Sodium Pyruvate, Theobroma Cacao (Cocoa) Seed Butter, Tocopherol

  • Questions?

    Call 1-844-241-5454 or visit Bactine.com

  • Distributed by:

    Distributed by: WellSpring Pharmaceutical Corporation
    Sarasota, FL 34243
    ©2023 WellSpring Pharmaceutical Corporation

    MONEY BACK GUARANTEE

    Bactine Max is FSA/HSA Eligible

  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

    NDC #: 65197-827-05

    NEW

    #1 PAIN RELIEVER*

    #1 ANTIBIOTIC MEDICINE**

    ANTIBIOTIC + MAX PAIN RELIEF with LIDOCAINE

    Kills Bacteria

    Prevents Infection

    Max Pain Relief

    NET WT 0.5 oz (14.2 g)

    NO STING - OINTMENT

    *Chosen by people that believe it is the most effective pain reliever active ingredient in WellSpring proprietary consumer research

    **Chosen by people that believe it is the most effective antibiotic active ingredient in WellSpring proprietary consumer research

    Carton Artwork Bactine Max Antibiotic

    CT82100A - Bactine Max Antibiotic

  • INGREDIENTS AND APPEARANCE
    BACTINE MAX ANTIBIOTIC AND LIDOCAINE MAX PAIN RELIEF 
    lidocaine ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65197-827
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS0.04 g  in 1 g
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC500 U  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 U  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    OLEA EUROPAEA FRUIT VOLATILE OIL (UNII: 8E7358CX1J)  
    GOSSYPIUM HERBACEUM SEED RESIN (UNII: X408487D9E)  
    SODIUM PYRUVATE (UNII: POD38AIF08)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    Product Characteristics
    Coloryellow (Smooth, pale yellow ointment) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65197-827-051 in 1 BOX01/15/2024
    114.2 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/15/2024
    Labeler - WellSpring Pharmaceutical Corporation (110999054)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!