Duet Base

Manufacturer
IBA | Morgan Gallacher Inc. DBA in Custom Chemical Formulators Inc.
Effective date
2025-11-26
Label type
OTC ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:45:18

Label at a glance#

ProductDuet Base
Active ingredientSODIUM CHLORITE
Label structure9 sections

Dosage and administration

1. It is recommended to wear nitrile or rubber gloves when handling a 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. 6.  Mix in a well ventilated area and a...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Chlorite 5.5%

Inert Ingredients

INACTIVE INGREDIENT SECTION

Stabilizers & Water

Mixing Directions

INDICATIONS & USAGE SECTION

1. It is recommended to wear nitrile or rubber gloves when handling a 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.

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 the label directions, a solution of acidified sodium chlorite is achieved in the ready-to-use product.

Warning

WARNINGS SECTION

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.

Danger

WARNINGS SECTION

Causes severe skin burns & eye damage.  

Harmful if swallowed.

May be corrosive to metals.

First Aid

OTHER SAFETY INFORMATION

If in Eyes: Rinse cautiously with water for several minutes.  Remove contact lenses if present & easy to do.  Continue rinsing for 15 minutes.  Get immediate medical advice/attention.

If Swallowed: Rinse mouth.  Do not induce vomitting.  Get immediate medical advice/attention.

If on Skin: Immediately remove all contaminated clothing.  Wash with plenty of water for 15 minutes.  If skin irritation occurs, get medical advice/attention.  Wash contaminated clothing before use.

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

Caution

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. 

Duet Base

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
29983-1100-2Duet Base4.09 kg in 1 BOTTLELIQUID4.092
29983-1100-6Duet Base61.36 kg in 1 DRUMLIQUID61.362
29983-1100-8Duet Base225 kg in 1 DRUMLIQUID2252
29983-1100-9Duet Base1125 kg in 1 CONTAINERLIQUID11252

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
29983-110029983-1100-6, 29983-1100-8, 29983-1100-9, 29983-1100-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORITEG538EBV4VFACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 11 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Doctor GuardStickSODIUM CHLORITEPure O2a39b49fd-9eac-73b4-e053-2995a90a180d2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
PURE O2STICKSODIUM CHLORITEPure O2a39a1e99-d714-645d-e053-2995a90a024c2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
EasyStickSODIUM CHLORITEPure O2a39b9ce6-a074-4165-e053-2995a90a277a2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
iSTICKSODIUM CHLORITEPure O2a6f7ea11-3cbe-6739-e053-2a95a90a41cf2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
NARYN CARE StickSODIUM CHLORITEPure O2a6fb2adf-5312-84c4-e053-2a95a90a5ded2023-11-16WarningsName fallback
generic name: SODIUM CHLORITE
D.PRO Pack SolidSODIUM CHLORITEPure O2c0289ea3-c592-0760-e053-2a95a90a0cfd2021-04-17WarningsName fallback
generic name: SODIUM CHLORITE
DEFENDERSTICKSODIUM CHLORITEPure O2c02915ef-e7fc-4811-e053-2a95a90a97702021-04-17WarningsName fallback
generic name: SODIUM CHLORITE
DEFENDER SIGNATURESODIUM CHLORITEPure O2c029345a-d44b-74db-e053-2995a90a1dbe2021-04-17WarningsName fallback
generic name: SODIUM CHLORITE
PURE O2 Pack-SolidSODIUM CHLORITEPure O2a397afb9-53a7-e6d8-e053-2a95a90a54d42020-08-29WarningsName fallback
generic name: SODIUM CHLORITE
QVE - SSODIUM CHLORITEPure O2acdeca69-4e20-9502-e053-2a95a90a53272020-08-14WarningsName fallback
generic name: SODIUM CHLORITE
V Doctor pure chlorine dioxideSODIUM CHLORITEPure O2a492a03c-c28e-fcd6-e053-2a95a90a65d42020-05-01WarningsName fallback
generic name: SODIUM CHLORITE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.