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Triple antibiotic plus pain relief - Medication Information

Product NDC Code 50066-202
Drug Name

Triple antibiotic plus pain relief

Type Brand
Pharm Class Aminoglycoside Antibacterial [EPC],
Aminoglycosides [CS],
Decreased Cell Wall Synthesis & Repair [PE],
Polymyxin-class Antibacterial [EPC],
Polymyxins [CS]
Active Ingredients
Bacitracin zinc 500 [usp'u]/g
Neomycin sulfate 3.5 mg/g
Polymyxin b sulfate 10000 [usp'u]/g
Pramoxine hydrochloride 10 mg/g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 1359350
Application Number M004
Labeler Name GENOMMA LAB USA, INC.
Packages
Package NDC Code Description
50066-202-01 1 tube in 1 carton (50066-202-01) / 28.4 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients (in each gram) Purpose Bacitracin zinc 500 units First aid antibiotic Neomycin sulfate 3.5 mg First aid antibiotic Polymyxin B sulfate 10,000 units First aid antibiotic Pramoxine HCl 10 mg External analgesic
Active ingredients (in each gram)Purpose
Bacitracin zinc 500 unitsFirst aid antibiotic
Neomycin sulfate 3.5 mgFirst aid antibiotic
Polymyxin B sulfate 10,000 unitsFirst aid antibiotic
Pramoxine HCl 10 mgExternal analgesic

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions adults and children 2 years of age and 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

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredient white petrolatum

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses first aid to help prevent infection and for the temporary relief of pain in minor: cuts scrapes burns

Purpose

Information about the drug product’s indications for use.
Active ingredients (in each gram) Purpose Bacitracin zinc 500 units First aid antibiotic Neomycin sulfate 3.5 mg First aid antibiotic Polymyxin B sulfate 10,000 units First aid antibiotic Pramoxine HCl 10 mg External analgesic
Active ingredients (in each gram)Purpose
Bacitracin zinc 500 unitsFirst aid antibiotic
Neomycin sulfate 3.5 mgFirst aid antibiotic
Polymyxin B sulfate 10,000 unitsFirst aid antibiotic
Pramoxine HCl 10 mgExternal analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
TRIPLE ANTIBIOTIC PLUS PAIN RELIEF Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride PETROLATUM BACITRACIN ZINC BACITRACIN NEOMYCIN SULFATE NEOMYCIN POLYMYXIN B SULFATE POLYMYXIN B PRAMOXINE HYDROCHLORIDE PRAMOXINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton cicatricure ® OPEN WOUND FOR MINOR CUTS, SCRAPES AND BURNS PAIN, ITCH & SCAR Triple Antibiotic Ointment Up to 24-Hour Infection Protection Maximum Strength: Infection Protection, Pain & Itch Relief Helps Healing Wounds, Minimizing the Appearance of Scars** FIRST AID ANTIBIOTIC PAIN RELIEVING OINTMENT Bacitracin Zinc – Neomycin Sulfate – Polyximin B Sulfate – Pramoxine HCl *Based on published studies. For best results use sterile bandage or gauze. **Preventing infection helps minimize appearance of scars. NET WT. 1 oz (28.4 g) triple-antibiotic

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Distributed by: Genomma Lab USA Inc. Houston, TX 77098

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have deep or puncture wounds animal bites serious burns

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if you are allergic to any of the ingredients in the eyes over large areas of the body

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Call toll free 1-877-994-3666 Monday to Friday 8am to 6pm, Central time

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
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

Storage and handling

Information about safe storage and handling of the drug product.
Other information store at 20° to 25°C (68° to 77°F) to open: unscrew cap, pull tab to remove foil seal see carton or tube crimp for lot number and expiration date

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API