Active Ingredient(S)
Ethyl Alcohol 60% v/v. Purpose: Antiseptic
Zero Hand Sanitizing Wipes
FDA Label NDC 80048-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by C&c Tech Co., Ltd. for the product Zero Hand Sanitizing Wipes (NDC 80048-001). 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(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
Antiseptic
Use
Hand Sanitizer to help reduce bacteria on the skin
Warnings
Flammable, keep away from heat or flame. For external use only.
Do Not Use
- on large areas of the body
- if you are allegic to any of the ingredients
Otc - When Using
When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash develops and continues 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
- For adults and children of 3 years and over, wet hands thoroughly with product and allow to dry.
- Supervise children under 6 years of age when using this product.
Other Information
- Store at room temperature
Inactive Ingredients
Purified water USP, Sodium Benzoate, Citric Acid, Disodium EDTA, Aloe Barbadensis Leaf Extract, Butylene Glycol
Package Label - Principal Display Panel
Label (Label)
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