BD PERSIST- povidone-iodine, alcohol solution 
Becton Dickinson and Company

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.

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17271-507 BD Persist

Drug Facts

Active Ingredient

Providone-Iodine 10% (w/w)

Ethyl Alcohol 70% (v/v)

Purpose

Antiseptic

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

50

Principal Display Panel – Carton Label

Principal Display Panel – Package Label

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

Principal Display Panel – Package Label
BD PERSIST 
povidone-iodine, alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17271-507
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE85 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
ETHYL ACETATE (UNII: 76845O8NMZ)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
UREA (UNII: 8W8T17847W)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:17271-507-0150 in 1 CARTON02/21/199609/30/2023
12 mL in 1 PACKAGE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
2NDC:17271-507-0225 in 1 CARTON02/21/199601/31/2023
27 mL in 1 PACKAGE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/21/199609/30/2023
Labeler - Becton Dickinson and Company (124987988)

Revised: 2/2023
Document Id: f49b7ea3-1101-75e0-e053-2a95a90ab354
Set id: a2af654b-8ec6-4990-8584-742ebc597639
Version: 6
Effective Time: 20230213
 
Becton Dickinson and Company