Label: GLADIATOR MAX BASE- chlorine dioxide teat dip liquid
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NDC Code(s):
48106-2046-1,
48106-2046-2,
48106-2046-3,
48106-2046-4, view more48106-2046-5, 48106-2046-6
- 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 February 28, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Claim of effectiveness.
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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.
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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
- General Storage
- Package label
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INGREDIENTS AND APPEARANCE
GLADIATOR MAX BASE
chlorine dioxide teat dip liquidProduct 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