COVER ALL MAX PART A- lactic acid solution

Cover All Max Part A by

Drug Labeling and Warnings

Cover All Max Part A by is a Animal medication manufactured, distributed, or labeled by Proactive Solutions USA, LLC, ProActive Solutions USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Cover All Max Part A

Cover All Max™ is a concentrated two part chlorine dioxide teat dip that will aid in the
prevention of the spread of mastitis causing organisms. Cover All Max™ contains alpha
hydroxy acids to aid in the exfoliation of teat skin and soften the hyperkeratosis at the teat
end.
MIXING INSTRUCTIONS:
Cover All Max™ is a two part concentrate that must be mixed prior to use. The mix ratio is
98:1:1. Mix enough Cover All Max™ to last for 24 hours. In a clean container add 98 parts
water, 1 part Cover All Max Part A™, and 1 part Cover All Max Part B™. Mix gently until
uniform and let stand for a minimum of 15 minutes. The mixed solution will reach or exceed
800ppm chlorine dioxide within 15 minutes. Keep the containers tightly closed and store in
a cool, dry area away from direct sunlight.
USE INSTRUCTIONS:
Pre-Dipping: If teats are dirty, pre-clean with a suitable udder wash and a single service
towel. Dip, spray, or foam each teat with Cover All Max™ chlorine dioxide. Leave on teats
a minimum of 15-30 seconds. Wipe teats dry with a single service towel and apply milker
units.
Post-Dipping: Immediately after milking, dip each teat with Cover All Max™ chlorine dioxide
teat dip. Allow to air dry.
Always use this mixture full strength. If product in dip cup becomes dirty, discard contents
and fill with a fresh solution.
If teat irritation occurs, discontinue use until irritation subsides. Consult your veterinarian if
irritation persists.
Ingredients:
Lactic Acid: 42.24%

Hazard statement(s):
Harmful if inhaled
Causes skin burns and eye damage
Causes serious eye damage
Precautionary statement(s):
Avoid breathing mist, vapors. Wear protective gloves, eye protection, and face protection.
Wash hands, forearms, and face thoroughly after handling. Take off contaminated clothing
and wash before reuse. Use only outdoors or in a well ventilated area. Call poison control
center if you feel unwell.
Hazards not otherwise classified: No additional information available
Storage and Disposal: Store in a cool, well-ventilated place away from heat. Protect from sunlight.
Store always product in container of same material as original container. Dispose of contents/container
to a hazardous or special waste collection point.
First Aid:
General: Call a poison center/doctor/physician if you feel unwell.
Skin Contact: Wash skin with plenty of water. Take off contaminated clothing. If skin
irritation occurs: Get medical advice/attention
Eye Contact: Rinse cautiously with water for several minutes. Remove contact lenses,
if present and easy to do. Continue rinsing. If eye irritation persist: Get medical advice/
attention.
Ingestion: Call a poison center/doctor/physician if you feel unwell
Inhalation: Remove person to fresh air and keep comfortable for breathing. Call a poison
center/doctor/physician if you feel unwell.
Most important symptoms/effects, acute and delayed:
Potential adverse human health effects and symptoms: Causes serious eye damage. Causes
severe skin burns.
Symptoms/effects after inhalation: Harmful if inhaled.
Symptoms/effects after skin contact: Burns.
Symptoms/effects after eye contact: Serious damage to eyes.

Cover All Max Part A

INGREDIENTS AND APPEARANCE

COVER ALL MAX PART A 
lactic acid solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 63927-4131
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	42.24 kg  in 100 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63927-4131-6	20.8 kg in 1 JUG
2	NDC: 63927-4131-2	62.4 kg in 1 DRUM
3	NDC: 63927-4131-3	228.9 kg in 1 DRUM
4	NDC: 63927-4131-4	1144.3 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
5	NDC: 63927-4131-5	1373.2 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/10/2025

Labeler - Proactive Solutions USA, LLC (029368225)

Registrant - ProActive Solutions USA, LLC (029368225)

Establishment
Name	Address	ID/FEI	Business Operations
ProActive Solutions USA, LLC		029368225	api manufacture, manufacture, label, pack, repack

Establishment
Name	Address	ID/FEI	Business Operations
ProActive Solutions USA, LLC		043147537	api manufacture, manufacture, label, pack, repack