FDA records indicate that there are no current recalls for this drug.
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Questions & Answers
Side Effects & Adverse Reactions
- For external use only
- contains alcohol which is flammable until dry
- if you are allergic to povidone iodine or ethyl alcohol
- to treat wounds or burns
- in eyes, mucus membranes
- on broken skin
- with electrocautery procedures
Stop use and ask a doctor if the insertion site becomes
- red
- irritated
- swollen
- painful
- infected
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- if you are allergic to povidone iodine or ethyl alcohol
- to treat wounds or burns
- in eyes, mucus membranes
- on broken skin
- with electrocautery procedures
Stop use and ask a doctor if the insertion site becomes
- red
- irritated
- swollen
- painful
- infected
Stop use and ask a doctor if the insertion site becomes
- red
- irritated
- swollen
- painful
- infected
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
- for preparation of the skin prior to percutaneous procedure
- helps reduce bacteria that potentially can cause skin infection
- does not contribute to skin irritation under an occlusive dressing with repeated applications
- reduces bacteria with routine site care for up to seven days
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Bd Persist Manufacturers
-
Becton Dickinson Infusion Therapy Systems Inc.
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