Active Ingredient(S)
Ethyl Alcohol 75%±5% v/v
Alcohol Disinfectant
FDA Label NDC 56084-025
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Rifeshow Cosmetics Co., Ltd. for the product Alcohol Disinfectant (NDC 56084-025). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
Alcohol Disinfectant to help reduce bacteria on skin.
Warnings
- For external use only.
- Flammable. Keep away from fire or flame.
Do Not Use
- in children less than 2 years of age
- on open skin wounds
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control center immediately.
Directions
For external use on the skin, it can also be sprayed on the surface of objects such as toilets, chairs, handrails, elevators, corridors, etc.
Other Information
- Store below 110℉(43℃)
- May discolor certain fabrics.
Inactive Ingredients
DEIONIZED WATER
Package Label - Principal Display Panel
930 mL NDC: 56084-025-01
930ml Label (930ml)
5000 mL NDC: 56084-025-02
5000ml Label (5000ml)
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