Label: XTRA BLU PART B- sodium chlorite solution solution
- NDC Code(s): 17307-3641-1, 17307-3641-2, 17307-3641-3, 17307-3641-4
- Packager: AgroChem Inc
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated September 23, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- XTRA BLU (PART B)
-
WARNINGS AND PRECAUTIONS
WARNING
AVOID FREEZING.
KEEP OUT OF DIRECT SUNLIGHT
CAUSES SERIOUS EYE IRRITATION.
KEEP OUT OF REACH OF CHILDREN.
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: Store locked up.
DISPOSAL: Dispose of contents/ container to an approved waste disposal plant
EMERGENCY TELEPHONE NUMBER (Chemtrec) 800-424-9300 CCN205494
- ACTIVE INGREDIENT
-
INSTRUCTIONS FOR USE
XTRA EcoBLU 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.
Directions:
NOTE: 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.
Directions:
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.
Teat Sprays can also be foamed or sprayed using recommended equipment.
Pre Dipping Use
Perform forestripping 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.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
XTRA BLU PART B
sodium chlorite solution solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:17307-3641 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE 0.021 kg in 1 kg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17307-3641-1 19 kg in 1 CONTAINER 2 NDC:17307-3641-2 57 kg in 1 DRUM 3 NDC:17307-3641-3 208 kg in 1 DRUM 4 NDC:17307-3641-4 1040 kg in 1 CONTAINER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/23/2020 Labeler - AgroChem Inc (805427700) Registrant - AgroChem Inc (805427700) Establishment Name Address ID/FEI Business Operations AgroChem Inc 805427700 api manufacture, manufacture