CONFIDENCE 0.10-2- iodine concentrate 
Universal

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Universal
Confidence 0.10-2

Confidence™ 0.10-2

A concentrate designed for use with an on-site blending unit / Un concentrado diseñado para usarse con una unidad de mezcla en el sitio

SI USTED NO PUEDE LEER ESTA ETIQUETA, POR FAVOR PIDA A ALGUIEN MAS QUE SE LA LEA ANTES DE USAR ESTE PRODUCTO

NOT FOR HUMAN USE

ACTIVE INGREDIENT:

Iodine * ................................... 0.42% w/w

After dilution according to directions

Iodine * .................................. 0.1%

* From Polyethoxy polypropoxy polyethoxy ethanol-iodine Complex

pH 5 minimum

FIRST AID:

Contact with product can cause irritation to eyes.  Avoid contact with eyes.

If in Eyes: Flush with water.  Remove contact lenses, if present, then continue flushing.  Get medical attention if irritation develops and persists.

If Swallowed:  Do not induce vomiting.  Call a physician or poison control center immediately.

STORAGE AND DISPOSAL:

Thoroughly rinse all measuring devices and store out of reach of children.  Avoid contact with food or feed.  Avoid storing near heat or open flame.  Keep from freezing.  If product is frozen, thaw in a warm room and mix well before using.  Keep container tightly closed when not in use.  Do not reuse empty container. Rinse empty container before disposing in a safe manner.

Read and understand all label instructions before using this product.  For additional information, refer to the Safety Data Sheet (SDS) available from your Universal representative.

DIRECTIONS FOR USE

GENERAL INSTRUCTIONS

DIRECTIONS FOR DILUTION

Automatic Blending

Manual Blending

PRE-DIPPING

POST DIPPING

Chemtrec Emergency Number

1-800-424-9300

NPE Free Formula

NET CONTENTS:        US GAL (        L)

LOT NO.:

EXP. DATE:

image description

CONFIDENCE 0.10-2 
iodine concentrate
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57906-469
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE.0042 kg  in 1 kg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
XANTHAN GUM (UNII: TTV12P4NEE)  
POLOXAMER 335 (UNII: G6DQL26D50)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM IODIDE (UNII: F5WR8N145C)  
DOCUSATE SODIUM (UNII: F05Q2T2JA0)  
SODIUM IODATE (UNII: U558PCS5Z9)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:57906-469-01216 kg in 1 DRUM
2NDC:57906-469-271080 kg in 1 TANK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/06/2021
Labeler - Universal (605831627)
Registrant - WestAgro, Inc. (069288728)
Establishment
NameAddressID/FEIBusiness Operations
WestAgro, Inc.147528723api manufacture, manufacture, label, pack
Establishment
NameAddressID/FEIBusiness Operations
K Klean dba WestAgro, Inc.002222368api manufacture, manufacture, label, pack
Establishment
NameAddressID/FEIBusiness Operations
WestAgro, Inc.095906480api manufacture, manufacture, label, pack
Establishment
NameAddressID/FEIBusiness Operations
WestAgro, Inc.069288728api manufacture, manufacture, pack, label

Revised: 1/2022
Document Id: c16e28c0-2613-46d3-86aa-2ca354c7e559
Set id: dec9269a-62b7-47ef-8be0-76577dc75ba8
Version: 2
Effective Time: 20220121
 
Universal