GLADIATOR MAX BASE- chlorine dioxide teat dip liquid

Gladiator Max Base by

Drug Labeling and Warnings

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

Drug Details [pdf]

Claim of effectiveness.

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, or GLADIATOR POSTMAX ACTIVATOR and water. In a well-ventillated area, mix 1 part GLADIATOR MAX BASE and 1 part GLADIATOR PREPMAX or POSTMAX ACTIVATOR and 20 parts water. Do not mix more product than will be used in 3 days.

First Aid

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.

Precautions & Hazards

PRECAUTION: Avoid eye contact. Do not ingest. Do not mix with any chemicals except as directed.

General Storage

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

Package label

INGREDIENTS AND APPEARANCE

GLADIATOR MAX BASE 
chlorine dioxide teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2046
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	5.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2046-1	3914 g in 1 PACKAGE
2	NDC: 48106-2046-2	19570 g in 1 PACKAGE
3	NDC: 48106-2046-3	58710 g in 1 PACKAGE
4	NDC: 48106-2046-4	117421 g in 1 PACKAGE
5	NDC: 48106-2046-5	215271 g in 1 PACKAGE
6	NDC: 48106-2046-6	1076359 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/28/2023

Labeler - BOUMATIC, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
BOUMATIC, LLC		124727400	api manufacture