QUALITY CHOICE POVIDONE IODINE- povidone iodine 10% liquid 
Chain Drug Market Association

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Quality Choice Povidone Iodine

Drug Facts

Active Ingredient

Povidone-Iodine 10%

(Equivalent to 1% titrable iodine)

Purpose

Antiseptic

Use

First aid antiseptic to prevent infection in minor cuts and burns.

Warnings

For External Use Only

Ask a doctor before use if you have

Stop use and consult a doctor if

When using this product do not

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

For preparation of the skin prior to surgery. Apply to the operative site prior to surgery.

As a first aid antiseptic. Clean the affected area. Apply a small amount on the area 1 to 3 times daily. May be covered with sterile bandage. If badaged, let it dry first.

Inactive Ingredients

Citric Acid, Disodium Phosphate, Glycerin, nonoxynol-9. Sodium Hydroxide and Purified Water.

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QUALITY CHOICE POVIDONE IODINE 
povidone iodine 10% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-230
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GLYCERIN (UNII: PDC6A3C0OX)  
NONOXYNOL-9 (UNII: 48Q180SH9T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-230-08237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/12/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/01/2008
Labeler - Chain Drug Market Association (011920774)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(63868-230) , analysis(63868-230) , pack(63868-230) , label(63868-230)

Revised: 12/2023
Document Id: 0cf49768-1bb7-199c-e063-6294a90a2fc3
Set id: 9fa49a3c-ad09-4d35-8cd9-e1a0f2da0d2d
Version: 6
Effective Time: 20231220
 
Chain Drug Market Association