GLADIATOR PREPMAX BASE- sodium chlorite pre dip liquid 
BouMatic, LLC

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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Gladiator PrepMax Base

 CAUTION

KEEP OUT OF REACH OF CHILDREN

NOT FOR HUMAN 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: Take off contaminated clothing. Rinse skin with soap and water. 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 except as directed.

STORAGE:Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix well before use.

SEE MATERIAL SAFETY DATA SHEET

Helps reduce the spread of organisms which may cause Mastitis

USE DIRECTIONS

NOT FOR HUMAN USE

FOR EXTERNAL USE ONLY

Do not mix with any chemicals other than GLADIATOR™ PREPMAX ACTIVATOR, and water.

In a well-ventilated area, mix 1 part GLADIATOR PREPMAX BASE and 1 part GLADIATOR PREPMAX ACTIVATOR and 20 parts water. Do not mix more product than will be used in 24-hours.

PRE-DIPPING:

Before milking, dip or spray entire teat with the mixed product. Wipe teats dry after application using single-service towels to avoid cross contamination.

image description

GLADIATOR PREPMAX BASE 
sodium chlorite pre dip liquid
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:48106-2031
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE74 g  in 10 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48106-2031-118.9 L in 1 DRUM
2NDC:48106-2031-256.8 L in 1 DRUM
3NDC:48106-2031-3208 L in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/17/2017
Labeler - BouMatic, LLC (124727400)
Registrant - BouMatic, LLC (124727400)
Establishment
NameAddressID/FEIBusiness Operations
boumatic080073197manufacture, api manufacture

Revised: 5/2017
Document Id: 719bbc49-7eba-4ad9-85f8-6e592452fc60
Set id: a7c1db85-0e6b-4381-95dc-a38bfce1ae52
Version: 1
Effective Time: 20170517
 
BouMatic, LLC