COVER ALL ULTRA PART B- sodium chlorite solution

Cover All Ultra Part B by

Drug Labeling and Warnings

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

Drug Details [pdf]

DESCRIPTION

Cover All Ultra™ is a concentrated two part chlorine dioxide teat dip that will aid in the
prevention of the spread of mastitis causing organisms. Cover All Ultra™ contains alpha
hydroxy acids to aid in the exfoliation of teat skin and soften the hyperkeratosis at the teat
end.
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 of Cover All Ultra Part A™ and 1 part Cover All Ultra Part B™ Mix gently 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:
Sodium Chlorite: 7.795%

Hazard statement(s):
Harmful if swallowed or if inhaled. Causes severe skin burns and eye damage. May cause
damage to organs (blood, kidneys, respiratory system) through prolonged or repeated
exposure. Toxic to aquatic life
Precautionary statement(s):
Wash hands, forearms and face thoroughly after handling. Do not eat, drink or smoke while
using this product. Wear protective gloves, clothing, and eye and face protection. Do not
breathe dusts or mists. Use only outdoors or in a well ventilated area. Avoid release to the
environment. Store locked up. Dispose of contents and container to a hazardous or special
waste collection point, in accordance with local, regional, national and/or international
regulation.
Hazards not otherwise classified: None Known
First Aid:
General: Call a poison center/doctor/physician if you feel unwell.
External: Rinse skin with water/shower. Remove/Take off immediately all contaminate
clothing.
Eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and
easy to do. Continue rinsing. If eye irritation persists: Get medical advice/attention.
Internal: Rinse mouth. Do not induce vomiting. Call a physician immediately.
Inhalation of vapors: Remove person to fresh air and keep comfortable for breathing. Call a
poison center/doctor/physician if you feel unwell.
Get medical attention immediately.
Most important symptoms/effects, acute and delayed:
Symptoms/effects after inhalation: Harmful if inhaled.
Symptoms/effects after skin contact: Burns.
Symptoms/effects after eye contact: Serious damage to eyes.
Symptoms/effects after ingestion: Harmful if swallowed. Burns
Other medical advice or treatment: Treat symptomatically.
Immediate medical attention and special treatment needed, if any:
Other medical advice or treatment: Treat symptomatically

Cover All Ultra Part B

INGREDIENTS AND APPEARANCE

COVER ALL ULTRA PART B 
sodium chlorite solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 63927-4124
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	7.795 kg  in 100 kg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63927-4124-6	20.18 kg in 1 JUG
2	NDC: 63927-4124-2	60.55 kg in 1 DRUM
3	NDC: 63927-4124-3	222.00 kg in 1 DRUM
4	NDC: 63927-4124-4	1110 kg in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
5	NDC: 63927-4124-5	1332 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