Nurinse Hand Sanitizer Q
f0744946-28d8-7977-e053-2a95a90a69a5
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Description
Benzalkonium Chloride 0.13%
Purpose
Antiseptic, Hand Sanitizer, Antibacterial
Medication Information
Purpose
Antiseptic, Hand Sanitizer, Antibacterial
Description
Benzalkonium Chloride 0.13%
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Section 50565-1
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Section 50566-9
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Section 50567-7
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Warnings
For external use only.
When using this product: Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop use and ask a Doctor: If skin irritation develops.
Keep out of reach of children.: If ingested, get medical help or call the Poison Control Center immediately.
Directions
- When using NuRinse Hand Sanitizer-Q, apply a palmful of the product to one hand and rub the product all over the surfaces of both hands until your hands are dry. Do not wipe away excess sanitizer. For children under 6, use only with adult supervision. Not recommended for infants.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
- Do not store above 120°F.
- May discolor some fabrics.
- Harmful to wood finishes and plastics.
Active Ingredient(s)
Benzalkonium Chloride 0.13%
Inactive Ingredients
- Purified water USP
- Humectant
- Moisturizer
- Foaming agent
Package Label Principal Display Panel
750mL is one bottle NDC: 77368-901-75
Structured Label Content
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Section 50565-1 (50565-1)
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Section 50566-9 (50566-9)
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Section 50567-7 (50567-7)
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Purpose
Antiseptic, Hand Sanitizer, Antibacterial
Warnings
For external use only.
When using this product: Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop use and ask a Doctor: If skin irritation develops.
Keep out of reach of children.: If ingested, get medical help or call the Poison Control Center immediately.
Directions
- When using NuRinse Hand Sanitizer-Q, apply a palmful of the product to one hand and rub the product all over the surfaces of both hands until your hands are dry. Do not wipe away excess sanitizer. For children under 6, use only with adult supervision. Not recommended for infants.
Do Not Use (Do not use)
- in children less than 2 months of age
- on open skin wounds
Other Information (Other information)
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
- Do not store above 120°F.
- May discolor some fabrics.
- Harmful to wood finishes and plastics.
Active Ingredient(s)
Benzalkonium Chloride 0.13%
Inactive Ingredients (Inactive ingredients)
- Purified water USP
- Humectant
- Moisturizer
- Foaming agent
Package Label Principal Display Panel (Package Label - Principal Display Panel)
750mL is one bottle NDC: 77368-901-75
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:00:26.967570 · Updated: 2026-03-14T23:00:52.351984