Parker Labs Redux Electrolyte Paste 67-05 | ECG & Defibrillation

Redux® Electrolyte Paste 67-05 – ECG, Short-Term Monitoring & Defibrillation

Redux Electrolyte Paste by Parker Laboratories is a water-based, abrasive, electrically conductive contact paste that is recommended for short-term patient monitoring, ECG/EKG procedures, and defibrillation.

Its conductive formulation helps create electrical contact between intact skin and compatible electromedical electrodes, paddles, or other patient-contact components. The abrasive characteristic distinguishes Redux Paste from smoother, non-abrasive products such as Redux Electrolyte Gel.

Redux Paste is also bacteriostatic and water-soluble. It is supplied in a 142 g/5 oz tube under Parker Laboratories' product number 67-05. The product is nonsterile and intended only for external use on intact, unbroken skin.

Important: Use Redux Paste only when the instructions for the ECG system, monitoring electrode, defibrillator, paddle, or related electromedical equipment permit a separately applied conductive paste. Do not add it beneath a pre-gelled disposable electrode or multifunction defibrillation pad unless the equipment manufacturer specifically directs that use. Parker instructs users to follow the connected electromedical device’s instructions for application. 

Product highlights

• Electrically conductive electrolyte paste

• Recommended for short-term monitoring

• Recommended for routine ECG/EKG procedures

• Recommended for compatible defibrillation procedures

• Water-based formulation

• Abrasive paste consistency

• Bacteriostatic

• Water-soluble

• Nonsterile

• For external use on intact, unbroken skin

• Removes with a moistened soft cloth

• Parker Laboratories product number 67-05

• Current manufacturer size: 142 g/5 oz

• Ten tubes per manufacturer box

• Five boxes or 50 tubes per manufacturer case

• No special handling requirements stated in the current IFU

• Protect from direct sunlight
  

Quick specifications

What is Redux Electrolyte Paste?

Redux Paste is a contact medium placed between intact skin and compatible electromedical equipment. It helps complete the electrical interface when the equipment requires a separately applied paste.

It does not generate, measure, or control the electrical signal or therapeutic energy. The connected ECG machine, patient monitor, or defibrillator controls those functions.

What does “abrasive” mean?

Redux Paste is formulated with an abrasive characteristic, unlike the non-abrasive Redux Gel. The page should not interpret “abrasive” as permission to scrub the skin aggressively or use the product as a general-purpose exfoliant.

The appropriate amount, pressure, and technique depend on the connected device, electrode, clinical protocol, and patient’s skin condition. Redux Paste is limited to intact, unbroken skin. 

It is also different from NuPrep Skin Prep Gel. NuPrep is a dedicated skin-preparation product used before compatible electrode placement. Redux Paste remains part of the conductive interface during an indicated procedure.

Bacteriostatic does not mean sterile

Parker identifies Redux Paste as both bacteriostatic and nonsterile. Therefore, the page should not claim or imply that the paste:

• Sterilizes skin

• Disinfects electrodes or paddles

• Creates a sterile field

• Prevents all bacterial growth

• Prevents procedure-related infection

• Is appropriate for broken skin

• Replaces infection-control procedures

Redux Paste has a bacteriostatic formulation. It is nonsterile and intended only for external use on intact, unbroken skin.

When Redux Paste may be appropriate:

Many contemporary ECG electrodes and multifunction defibrillation pads are already pre-gelled. Additional paste can interfere with adhesion or alter the intended interface, so it should not be added automatically. This follows the instruction to use Redux according to the connected equipment’s directions.

What Redux Paste is not

Redux Paste vs. Redux Gel vs. Redux Creme

Choose Redux Paste when:

• Short-term monitoring is part of the workflow.

• The equipment calls for an abrasive conductive paste.

• Routine ECG is being performed with compatible equipment.

• A defibrillator or paddle system specifically permits a separate paste.

• A bacteriostatic paste formulation is preferred.

Comparison with other conductive media

Redux Paste vs. Ten20

Redux Paste and Ten20 are both called “conductive paste,” but their applications differ substantially.

Do not substitute Ten20 Conductive Paste for Redux Paste in a defibrillation workflow. Likewise, Redux Paste should not be an EEG cup-electrode adhesive. 

For additional neurodiagnostic context, see our Ten20 vs. NuPrep: When to Use Each Product.

How to use Redux Electrolyte Paste

There is not one specified universal application amount because use depends on the connected electromedical equipment. The following product-page workflow stays within the manufacturer’s directions.

1. Confirm equipment compatibility. Verify that the monitor, ECG electrode, defibrillator, or paddle system permits or requires a separate conductive paste.

2. Inspect the tube. Do not use the product if the container is damaged or contamination is visible or suspected.

3. Inspect the application site. Apply only to intact, unbroken skin.

4. Avoid contaminating the tube. Do not let the dispensing tip touch the patient, staff, electrode, paddle, instrument, glove, or another surface.

5. Apply according to the equipment instructions. Use only the amount and placement specified by the device manufacturer or facility procedure.

6. Perform the procedure. Follow all ECG, monitoring, or defibrillator operating instructions.

7. Remove remaining paste. Parker states that Redux can be removed with a moistened soft cloth.

8. Close and store the tube. Protect the product from direct sunlight.

Defibrillation considerations

Redux Paste is indicated for defibrillation, but that does not mean it should be added to every defibrillator setup.

Defibrillation equipment controls energy delivery; Redux Paste only provides a conductive interface. Application amount, paddle placement, energy selection, charging, discharge, and safety procedures must follow the defibrillator manufacturer’s instructions. 

Infection-control and tube handling

Redux Paste is sold in a multiuse tube. The manufacturer specifically instructs users not to let the tube tip contact patients, staff, or instruments.

Recommended handling language:

• Dispense without touching the treatment surface.

• Do not return unused paste to the tube.

• Replace the cap promptly.

• Discard the product if contamination is suspected.

• Follow the facility’s policy for nonsterile multiuse contact media.

• Do not use Redux Paste when a procedure requires sterile contact media.

• Do not apply it to broken or compromised skin.

Safety, storage, and disposal

Nonsterile. For external use only on intact, unbroken skin. Use Redux Paste only as permitted by the connected electromedical equipment’s instructions. Discard the product if the tube is damaged or contamination is suspected. Do not allow the dispensing tip to touch the patient, staff, electrodes, paddles, or instruments.

Frequently asked questions

What is Redux Electrolyte Paste used for?

Redux Paste for short-term monitoring, routine ECG procedures, and defibrillation. The connected device instructions must permit a separately applied conductive paste.

Who manufactures Redux Paste?

Redux Paste is manufactured by Parker Laboratories, Inc. 

What is the manufacturer's product number?

67-05. 

Is the tube 4 oz or 5 oz?

142 g/5 oz.

Is Redux Paste sterile?

No. IFU identifies it as nonsterile. 

Is Redux Paste bacteriostatic?

Yes. It is bacteriostatic. This does not mean that the paste is sterile or that it disinfects the skin or equipment. 

Is Redux Paste abrasive?

Yes, it is a water-based abrasive paste. 

Is it water-soluble?

Yes. Redux Paste is water-soluble, and the IFU says residue can be removed with a moistened soft cloth. 

Can Redux Paste be used for ECG or EKG?

Yes. Routine ECG is one of its manufacturer-listed applications. 

Can it be used for short-term monitoring?

Yes. Short-term monitoring is specifically included in the current indication. 

Can it be used for defibrillation?

Yes, when the defibrillator, paddles, or electrodes specifically permit or require a separate conductive paste. Do not add it to pre-gelled multifunction pads unless directed by their instructions. 

Is Redux Paste an adhesive?

It does not identify Redux Paste as an adhesive. It will not hold electrodes in place.

For adhesive conductivity, compare Tensive Conductive Adhesive Gel. For EEG cup electrodes, Ten20 conductive paste is a better choice. 

Is it the same as Redux Gel?

No. Redux Paste is abrasive, bacteriostatic, and indicated for short-term monitoring, ECG, and defibrillation. Redux Gel is non-abrasive and indicated for routine ECG and defibrillation. 

Is it the same as Redux Creme?

No. Redux Creme is a bacteriostatic conductive cream for routine ECG and is not indicated for defibrillation.

Can it be used for EEG cup electrodes?

Redux Paste is not specifically indicated as an adhesive neurodiagnostic cup electrode paste. Ten20 Conductive Paste is the more appropriate Balego product for EEG, evoked potentials, PSG, MSLT, and related non-gelled neurodiagnostic electrodes.

Can it be used for TENS or NMES?

TENS and NMES are not included in the current Redux Paste indications reviewed. Use the electrode and stimulation-device instructions to select an appropriate contact medium. Spectra 360 Electrode Gel is specifically positioned for compatible TENS applications and conductive rubber or carbon electrodes. 

Can Redux Paste be applied to broken skin?

No. Parker limits it to external use on intact, unbroken skin. 

How is it removed?

Parker says Redux products can be removed with a moistened soft cloth. 

How should it be stored?

Protect the product from direct sunlight and follow any additional instructions printed on the current tube or carton. 

How many tubes are in a manufacturer case?

Parker packages ten 5 oz tubes per box and five boxes per case, for a total of 50 tubes per manufacturer's case.