BD PERSIST

Dosage form: solution
Ingredients: povidone-iodine 85mg in 1mL, alcohol 0.7mL in 1mL
Labeler: Becton, Dickinson and Company
NDC code: 17271-507

Medically reviewed by Drugs.com. Last updated on Sep 3, 2024.

Drug Facts

Active Ingredient

Providone-Iodine 10% (w/w)

Ethyl Alcohol 70% (v/v)

Purpose

Antiseptic

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

Warnings

For external use only
contains alcohol which is flammable until dry
Single use only

Do not use

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.

Directions

apply with friction for 30 seconds
allow to dry
do not blot or wipe away

Inactive ingredients

acrylates copolymer, ethyl alcohol, isopropyl myristate, urea, water

Principal Display Panel – Carton Label

BD Persist™
Skin Prep

One Step Application
One Swab Stick
Non-sterile solution

Principal Display Panel – Package Label

BD Persist™ Skin Prep
1 Swab Stick • Non-sterile solution REF 386401 NDC 17271-507-01

BD PERSIST
povidone-iodine, alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:17271-507
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
povidone-iodine (iodine)	iodine	85 mg in 1 mL
alcohol (alcohol)	alcohol	0.7 mL in 1 mL

Inactive Ingredients
Ingredient Name	Strength
carbomer copolymer Type A
ethyl acetate
isopropyl myristate
urea
water

Packaging
#	Item Code	Package Description
1	NDC:17271-507-01	50 PACKAGE in 1 CARTON
1		2 mL in 1 PACKAGE
2	NDC:17271-507-02	25 PACKAGE in 1 CARTON
2		7 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/21/1996

Labeler - Becton, Dickinson and Company (124987988)

Establishment
Name	Address	ID/FEI	Operations
Becton, Dickinson and Company		124987988	MANUFACTURE(17271-507)

Revised: 09/2012

Document Id: 4bf7e98e-e62c-4d8e-9ae5-9054a495e312

Set id: a2af654b-8ec6-4990-8584-742ebc597639

Version: 4

Effective Time: 20120913

Becton, Dickinson and Company

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer