POVIDONE IODINE- povidone iodine 10% liquid 
Humco Holding Group, Inc.

----------

Private Label Povidone Iodine

Drug Facts

Active Ingredient

Povidone-Iodine 10%

(1% available iodine)

Purpose

First Aid 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

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.

Other information

store at room temperature, 20-25C (68-77F)

Inactive Ingredients

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

Sunmark Label

8 fl oz

SM 8

16 fl oz

SM 16

Good Neighbor Label

GNPPov.jpgGNP

Leader Label

LDRPov.jpgLeader

Quality Choice Label

QCPov.jpgQC

Select Brand Label

SB

Publix Label

Publix

Premier Value Label

PV

Fred's Label

Freds

DDM Label

DDM

Rite Aid Label

RAPov.jpgRA

CVS Label

CVS

Vida MIaa Label

VM

HEB Label

HEB

Health Mart Label

HMPov.jpgHM

Purdue Betadine Label

Purdue Betadine 10.jpg

Top Care Label

Top Care PovidoneTCPov.jpg

POVIDONE IODINE 
povidone iodine 10% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-9123
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:0395-9123-98237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/14/2017
2NDC:0395-9123-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/14/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/01/2008
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114manufacture(0395-9123) , analysis(0395-9123) , pack(0395-9123) , label(0395-9123)

Revised: 12/2023
Document Id: 0c936cb3-8393-0603-e063-6394a90a0640
Set id: 6064c23b-7c15-208d-e053-2991aa0a00f6
Version: 7
Effective Time: 20231215
 
Humco Holding Group, Inc.