Active Ingredient
Alcohol Denat. 75% v/v.
Mu Instant Hand Sanitizer
FDA Label NDC 78422-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Royal Union Co., Ltd. for the product Mu Instant Hand Sanitizer (NDC 78422-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- to decrease bacteria on the skin that could cause disease.
- recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame.
When using this product, avoid contact with broken skin, do not inhale or ingest.
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if
- irritation or redness develops
- condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
•Place enough product on hands to cover all surfaces. Rub hands together until dry.
•Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Other information
- Do not store above 105°F.
- May discolor some fabrics.
- Harmful to wood finishes and plastics.
Inactive Ingredients
Water, acrylic acid homopolymer, Butane-1,3-diol, 1,1-propanediol, monoisobutanolamine, Fragrance
Package Label - Principal Display Panel
Product Label (Label)
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