Label: EQUALINE FIRST AID ANTIBIOTIC- bacitracin, neomycin, polymyxin b, pramoxine hcl ointment

  • NDC Code(s): 41163-040-58, 41163-040-64
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 August 1, 2023

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

View All Sections
  • Active ingredient (in each gram)

    Bacitracin zinc 500 units

    Neomycin sulfate equivalent to 3.5 mg of neomycin base

    Polymyxin B 10,000 units as polymyxin B sulfate

    Pramoxine HCl 10 mg

  • Purpose

    First aid antibiotic

    External analgesic

  • Uses

    first aid to help prevent infection and for temporary relief of pain or discomfort in minor:

    •
    cuts
    •
    scrapes
    •
    burns
  • Warnings

    For external use only.

    Do not use

    •
    if you are allergic to any of the ingredients
    •
    in the eyes
    •
    over large areas of the body

    Ask a doctor before use if you have

    •
    deep or puncture wounds
    •
    animal bites
    •
    serious burns

    Stop use and ask a doctor if

    •
    you need to use longer than 1 week
    •
    condition persists or gets worse
    •
    symptoms persist for more than 1 week, or clear up and occur again within a few days
    •
    rash or other allergic reaction develops

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

  • Directions

    •
    adults and children 2 years of age or older:
    •
    clean the affected area
    •
    apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
    •
    may be covered with a sterile bandage
    •
    children under 2 years of age: ask a doctor
  • Other information

    •
    store at 20-25°C (68-77°F)
  • Inactive ingredients

    white petrolatum

  • Questions or comments?

    1-877-932-7948

  • Principal Display Panel

    compare to Neosporin® active ingredients

    helps prevent infection in minor:

    cuts

    scrapes

    burns

    first aid antibiotic pain relieving ointment

    compare to Neosporin® active ingredients

    maximum strength ointment

    first aid antibiotic + pain relief

    bacitracin zinc – neomycin sulfate – polymyxin B sulfate – pramoxine HCl

    first aid antibiotic/pain relieving ointment

    NET WT 0.5 OZ (14g)

    Equaline first aid antibiotic Image 1
    Equaline first aid antibiotic Image 2
  • INGREDIENTS AND APPEARANCE
    EQUALINE FIRST AID ANTIBIOTIC 
    bacitracin, neomycin, polymyxin b, pramoxine hcl ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    ColorYELLOW (Translucent) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-040-641 in 1 CARTON04/02/2015
    128 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:41163-040-581 in 1 CARTON04/02/201502/28/2021
    214 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B04/02/2015
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
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!