Label: BLUEMAX PREMIUM EU- chlorine dioxide liquid
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NDC Code(s):
48106-1195-1,
48106-1195-2,
48106-1195-3,
48106-1195-4, view more48106-1195-5, 48106-1195-6
- Packager: BouMatic, LLC
- Category: OTC ANIMAL DRUG LABEL
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 January 1, 2013
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
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- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL
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INDICATIONS & USAGE
CHLORINE DIOXIDE SOLUTION
READY-TO-USE
INSTRUCTIONS FOR USE :
NOT FOR HUMAN USE.
FOR EXTERNAL AND PROFESSIONAL USE ONLY.
Before milking, treat the entire teat with this product, let act a
few seconds and wipe teats dry using single-use towels to
avoid any contamination of milk.
After milking, treat the entire teat with this product. Allow to
air dry.
Note: Replace the visibly dirty solution with fresh solution.
Do not return unused product to original container.
EMOLLIENTS 15%
ACTIVE SUBSTANCE (0,9 % Chlorine Dioxide)
Caution: the equipment must be adapted to contact with
chlorine dioxide -
PEDIATRIC USE
FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for 15-20 minutes.
Remove contact lenses, if present after the first 5 minutes, then continue rinsing. Contact a
physician immediately.
If swallowed: Have person sip a glass of water if able to swallow. Do not give anything to
an unconscious person. Do not induce vomiting. Contact a physician immediately.
If breathing difficulty occurs: Move person to fresh air. Contact a physician
immediately.
If on skin: If irritation develops and persists, contact a physician.
Have the product container or label with you when going for treatment, calling a physician,
the emergency number listed on this label or MSDS, or a poison control center.
PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals. Only use
in one ventilated areas.
STORAGE: Store in a closed container away from sources of heat. If product becomes
frozen, thaw and mix well before use.
Remember these industry guidelines:
Always use caution when introducing your cows to a new product.
Replace applicator. When introducing a new solution to a dairy herd, always replace
applicator to prevent the new solution from mixing with the old applicator. If pumps are
used, lines should be flushed with hot water to clean out any residues of the old solution.
Aggressively remove keratin and exfoliated skin from teats
A temporary exfoliation of dead teat skin is common after new solution are introduced. Be
sure to aggressively clean teats to remove exfoliated skin and clean teat ends to insure that
the dead skin is removed.
Monitor cows for changes in skin condition
Many solutions are designed with emollients and other skin conditioning ingredients to
maintain healthy teat skin and fight germs. Rare teat skin reactions due to allergic or
environmental conditions may occur. Closely monitor teat skin whenever a new solution is
introduced. If unusual skin conditions are found, monitor closely and, if persistent, replace
solution with one containing a different germicide and/or emollient formula -
INGREDIENTS AND APPEARANCE
BLUEMAX PREMIUM EU
chlorine dioxide liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:48106-1195 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE 32 g in 10 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:48106-1195-1 3.8 L in 1 DRUM 2 NDC:48106-1195-2 18.9 L in 1 DRUM 3 NDC:48106-1195-3 56.8 L in 1 DRUM 4 NDC:48106-1195-4 114 L in 1 DRUM 5 NDC:48106-1195-5 208 L in 1 DRUM 6 NDC:48106-1195-6 1040 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/01/2013 Labeler - BouMatic, LLC (124727400) Registrant - BouMatic, LLC (124727400) Establishment Name Address ID/FEI Business Operations BouMatic, LLC 124727400 manufacture, api manufacture