XTRA BLU CONC. PART B- sodium chlorite solution

XTRA BLU Conc. Part B by

Drug Labeling and Warnings

XTRA BLU Conc. Part B by is a Animal medication manufactured, distributed, or labeled by AgroChem USA, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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XTRA BLU (1:2) Conc. (Part B)

WARNINGS

WARNING

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

WARNINGS AND PRECAUTIONS

NOT FOR HUMAN USE.

AVOID FREEZING.

KEEP OUT OF DIRECT SUNLIGHT.

CAUSES SERIOUS EYE IRRITATION.

FOR FARM AND INDUSTRIAL USE ONLY.

PREVENTION:  Wash skin thoroughly after handling. Wear eye protection/ face protection.

FIRST AID / RESPONSE: 

IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists:  Get medical advice/ attention.

STORAGE AND HANDLING

STORAGE:  Store locked up.                       

DISPOSAL: Dispose of contents/ container to an approved waste disposal plant

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NDC: 17307-3013-3

NET CONTENTS:  55 GALLON (208.2L)

LOT:

EXP. DATE:

ACTIVE INGREDIENT

ACTIVE  INGREDIENT (when  diluted 1:2): Sodium  Chlorite  0.65%

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XTRA  BLU  is a  two- part  Chlorine  Dioxide  teat  dip  that  can   be  effectively  used  to  reduce  the  spread  of  mastitis  causing  organisms.  Recommended  for  pre  and   post  milking  applications.

INSTRUCTIONS FOR USE

DIRECTIONS:

IMPORTANT -  THIS  IS  A  CONCENTRATE  AND  MUST  BE  DILUTED  1:2.   Mix  by  volume.  After  dilution,  part  A   must   be   mixed  prior  to  use.  MIX  PART  A   &  PART  B  IN  EQUAL  PARTS.  CREATES  CHLORINE  DIOXIDE.   Reaches  minimum  Chlorine  Dioxide  levels  within  15  minutes  of  mixing.  Will  maintain  minimum  Chlorine  Dioxide  levels  for  up  to  24  hours.  It   is  recommended  to  replace  with  freshly  mixed  XTRA  BLU   after  24  hours.

General  Use

Use  a  teat  dip  cup  to  apply.  Clean  dip  cup   just  prior to  use.  If  cow’s  teats  are  sore  or  chapped,  consult  a   veterinarian   before  starting  or continuing  to  use  teat  dip.  If  transferred  from  this  container  to  any  other,  make  sure  that  the  other  container  is  thoroughly  pre- cleaned  and   bears  the  proper container  labeling  for  this  product. 

If  product  in  dip  cup  becomes  visibly  dirty,  discard  contents  and  replenish  with  undiluted  product.  Do   not  reuse  or  return  any  unused  product  to  the  original  container.  This  product  can  also  be  foamed  or  sprayed  using  recommended equipment

Pre Dipping Use

Perform forest ripping and inspect teats for clinical mastitis.

Pre-wash teats thoroughly just prior milking with appropriate udder wash solution or pre-milking teat dip. Teats should then be dried with single-service towels.

Just before each cow is milked, dip, foam, or spray, each teat full-length into the teat dip or foam cup containing product.

Allow product to stand for 30 seconds.

Wipe teats dry after dipping, using single-service towels to avoid contamination of milk.

Post Dipping Use

Immediately after each milking, use product.

Dip each teat full-length into the teat dip cup containing product. Allow to air dry. Do not wipe.

If outside temperature is below freezing, allow to air dry on the teat before cow leaves the parlor.

Extended Use

When a cow is being dried off, the teats should be dipped in product, once a day for 3-4 days after the last milking.

Dipping should be resumed at least twice daily one week before calving.

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Manufactured By:

AgroChem USA, LLC 26 Freedom Way Saratoga Springs, NY 12866 (518)226-4850

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XTRA BLU CONC. PART B 
sodium chlorite solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 17307-3013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	0.06318 kg  in 1 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17307-3013-1	19 kg in 1 CONTAINER
2	NDC: 17307-3013-2	57 kg in 1 PACKAGE
3	NDC: 17307-3013-3	208 kg in 1 DRUM
4	NDC: 17307-3013-4	1003 kg in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/26/2024

Labeler - AgroChem USA, LLC. (118336116)

Registrant - AgroChem USA, LLC. (118336116)

Establishment
Name	Address	ID/FEI	Business Operations
AgroChem USA, LLC.		118336116	api manufacture, manufacture, analysis, label, pack