Active Ingredient(S)
Alcohol 70% v/v. Purpose: Antiseptic
70% Alcohol Hand Sanitzer
FDA Label NDC 75021-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by D Zone Imports, Llc for the product 70% Alcohol Hand Sanitzer (NDC 75021-003). 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, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame
When Using This Product
Avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop Use And Ask A Doctor If
irritation or redness develops
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center.
Directions
- Wet hands thoroughly with product and rub into skin until dry.
- Children under 6 years of age should be supervised by an adult when using.
Other Information
- Store at room temperature
- May discolor certain fabrics
Inactive Ingredients
Deionized Water, Glycerol, Carbopol, Triethanolamine
Package Label - Principal Display Panel
60 mL NDC: 75021-003-01
Pdp (75021 003 01)
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