DUET BASE- sodium chlorite solution

DUET BASE by

Drug Labeling and Warnings

DUET BASE by is a Animal medication manufactured, distributed, or labeled by IBA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Contains 6.25% Sodium Chlorite 80%

(PROVIDES A FULL 5% AVAILABLE SODIUM CHLORITE)...........5%

INDICATIONS AND USAGE

MIXING DIRECTIONS

1. It is recommended to wear nitrile or rubber gloves when handling this concentrate to avoid staining hands.

2. Always mix solutions into a clean, well labeled, non-metalic, empty container.

3. Fill empty container with proper amount of cold, soft water.

4. Add proper amount of DUET Base to container as directed.

5. Add proper amount of DUET Activator to container as directed. Mix until the color is uniform throughout.

6. Mix in a well ventilated area and avoid breathing fumes.

7. Use mixed solution within 12 hours.

8. When DUET BASE and DUET ACTIVATOR are mixed properly according to label directions a solution of acidified sodium chlorite is achieved in the ready-to-use product.

RECOMMENDED PROCEDURES FOR TEAT SANITATION

A. PRE-MILKING (PRE-DIPPING)

1. Remove visible soils from the teats.

2. Observe foremilk by strippping two or three streams of milk into a strip cup.

3. Dip or Spray the cow's teats full lenth with READY-TO-USE DUETTEAT DIP.

4. Waut at least 15-30 seconds

5. Remove all teat dip by thoroughly drying the teats, teat orifices and udder with a clean, single service paper towel(s) to avoid contamination of milk.

6, Attach milking unit
POST-MILKING (POST DIPPING)

Immediately after milking, dip or spray all teats full length with READY-TO-USE DUET TEAT DIP. Ensure good coverage of all sides of the teats and teat orifices. Allow to dry. Do not wipe. Do not turn cows out in freezing weather until teat dip is completely dry.

WARNING

1. Use teat dip applicators made of plastic or other non-corrosive materials. Do not use cups made of aluminum.

2.When solution in the teat dip cup becomes dirty discard remaining contents and refill cup with fresh teat dip.

3. Do not use this product for cleaning or sanitizing equipment.

4. Wash teat dip cups after each milking.

5. Protect this product from freezing.

FIRST AID PROCEDURES

Keep out of reachof children. Read label before use. Do not breath fumes/gas/mist/vapors or spray. Do not get in eyes, on skin, or on clothing. Wear rubber gloves, chemical goggles, face shield and rubber apron. Wash hands thoroughly after handling. Take any precation to avoid mixing with chlorinated or ammoniated products. do not mix with any other chemicals.

IF IN EYES: RINSE CAUSTIOUSLY WITH FRESH,TEPID WATER FOR SEVERAL MINUTES.REMOVE CONTACT LENSES IF PRESENT AND EASY TO DO. CONTINUE RINSING FOR 15 MINUTES. GET IMMEDIATE MEDICAL ADVICE/ATTENTION.

IF ON SKIN: Immediately remove all contaminated clothing. Wash skin with plenty of water for 15 minutes. If skin irritation occurs, get medical advice/attention. Wash contaminated clothing before reuse.

IF SWALLOWED: DO NOT INDUCE VOMITING.NEVER GIVE ANYTHING BY MOUTH TO AN UNCONSCIOUS PERSON.DRINK LARGE AMOUNTS OF WATER. IF VOMITING OCCURS, KEEP AIRWAYS OPEN. KEEP HEAD LAWER THAN THE HIPS TO PREVENT ASPIRATION INTO THE LUNGS. GET IMMEDIATE MEDICAL ADVISE/ATTENTION.

IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. If experiencing respiratory symptoms get medical advice/attention immediately.

ALWAYS SEEK IMMEDIATE MEDICAL ATTENTION

FOR MEDICAL EMERGENCIES CALL 1-800-424-9300

DUET BASE

INGREDIENTS AND APPEARANCE

DUET BASE 
sodium chlorite solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 29983-0106
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 g  in 1 L

Product Characteristics
Color	white (CLEAR)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29983-0106-4	18.9 L in 1 DRUM
2	NDC: 29983-0106-6	56.7 L in 1 DRUM
3	NDC: 29983-0106-8	207.9 L in 1 DRUM
4	NDC: 29983-0106-9	1039.5 L in 1 DRUM

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/03/2023

Labeler - IBA (019494160)