GLADIATOR PREPMAX BASE- sodium chlorite pre dip liquid

Gladiator PrepMax Base by

Drug Labeling and Warnings

Gladiator PrepMax Base by is a Animal medication manufactured, distributed, or labeled by BouMatic, LLC, boumatic. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WARNINGS AND PRECAUTIONS

 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

INDICATIONS & USAGE

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GLADIATOR PREPMAX BASE 
sodium chlorite pre dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2031
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	74 g  in 10 L

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2031-1	18.9 L in 1 DRUM
2	NDC: 48106-2031-2	56.8 L in 1 DRUM
3	NDC: 48106-2031-3	208 L in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/17/2017

Labeler - BouMatic, LLC (124727400)

Registrant - BouMatic, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
boumatic		080073197	manufacture, api manufacture