RenaKare Potassium Gluconate Powder

Neogen Corporation

Revision date : 2025-04-14

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GHS08
Health risk rating 5
Safety risk rating 1
Environmental risk rating 1

General Information

Version

2.0

Revision date

2025-04-14

Product name

RenaKare Potassium Gluconate Powder

1.2.1 Relevant identified uses

Animal health

1.2.2. Uses advised against

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian

supplier name

Neogen Corporation

Manufacturer Name

Neogen Corporation

Emergency telephone

1-800-498-5743, 1-651-523-0318, 1-800-424-9300, 1-703-527-3887

Icons in SDS

GHS08 M004 M009 M010

Company Information

company name

Neogen Corporation

e-mail address of the competent person responsible for the Safety Data Sheet

sds@neogen.com

GHS Information

Signal word

Danger

Hazard Codes

Hazard statements (CLP)

H334

Hazard statements

Code

Statements

H334

May cause allergy or asthma symptoms or breathing difficulties if inhaled

Section 2

SECTION 2: Hazards identification

GHS US classification Classification of the substance or mixture GHS US classification Respiratory sensitization, Category 1 H334 May cause allergy or asthma symptoms or breathing difficulties if inhaled Full text of H statements see section 16

2.2 Label elements

GHS US labeling

Signal word

Danger

Hazard statements

H334 - May cause allergy or asthma symptoms or breathing difficulties if inhaled

Precautionary statements

P261 - Avoid breathing dust, fume, gas, mist, vapors, spray. P284 - Wear respiratory protection. P304+P340 - If inhaled: Remove person to fresh air and keep comfortable for breathing. P342+P311 - If experiencing respiratory symptoms: Call a poison center or doctor. P501 - Dispose of contents and/or container to hazardous or special waste collection point, in accordance with local, regional, national and/or international regulations. 2.3. Hazards associated with known or reasonably anticipated uses No additional information available

2.3 Other hazards

No additional information available 2.5. Unknown acute toxicity 26% of the mixture consists of ingredient(s) of unknown acute toxicity (Oral) 98% of the mixture consists of ingredient(s) of unknown acute toxicity (Dermal) 100% of the mixture consists of ingredient(s) of unknown acute toxicity (Inhalation (Dust/Mist))

2.1 Classification of the substance or mixture

Respiratory sensitization, Category 1 H334 May cause allergy or asthma symptoms or breathing difficulties if inhaled. Full text of H statements : see section 16 2.2. Label elements

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