COVER ALL ULTRA PART A- lactic acid solution

Cover All Ultra Part A by

Drug Labeling and Warnings

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

Drug Details [pdf]

Cover All Ultra Part A

MIXING INSTRUCTIONS:
Cover All Ultra™ is a two part concentrate that must be mixed prior to use. The mix ratio is
56:1:1. Mix enough Cover All Ultra™ to last for 24 hours. In a clean container add 56 parts
water, 1 part Cover All Ultra Part A™, and 1 part Cover All Ultra 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 Ultra™ Exp. 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 Ultra™ Exp. 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: 24.5%

Hazard statement(s):
Harmful if inhaled
Causes skin irritation
Causes serious eye irritation
Precautionary statement(s):
Avoid breathing dust,fume,gas,mist, vapors, or spray. Use only outdoors or in a well
ventilated area. Wear protective gloves and wash hands, face, thoroughly after handling.
Take off contaminated clothing and wash before reuse. Call a poison center or doctor if you
feel unwell.Specific treatment (see supplemental first aid instructions)
Hazards not otherwise classified: No additional information available.
Storage and Disposal: Keep 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 and
container to a hazardous or special waste collection point, in accordance with local, regional,
national and/or international regulation.
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: Moderate irritant for eyes
Symptoms/effects after inhalation: Harmful if inhaled
Symptoms/effects after skin contact: Irritation
Symptoms/effects after eye contact: Eye irritation
Symptoms/effects after ingestion: May be harmful if swallowed
Other medical advice or treatment: Treat symptomatically

Cover All Ultra Part A

INGREDIENTS AND APPEARANCE

COVER ALL ULTRA PART A 
lactic acid solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 63927-4123
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	24.5 kg  in 100 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63927-4123-6	20.81 kg in 1 JUG
2	NDC: 63927-4123-2	62.42 kg in 1 DRUM
3	NDC: 63927-4123-3	228.87 kg in 1 DRUM
4	NDC: 63927-4123-4	1144.35 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
5	NDC: 63927-4123-5	1373.213 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