Active Ingredient(S)
Ethyl Alcohol 70% Purpose: Antimicrobial
Dailygard Hand Sanitizer
FDA Label NDC 75571-004
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 Belair Trading Co., Ltd. for the product Dailygard Hand Sanitizer (NDC 75571-004). 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, uses, warnings, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
Use(s)
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
Warnings
For external use only. Flammable, Keep away from heat or flame
Do not use
- on infants
- on open skin wounds
- Keep out of eyes, ears, and mouth
- In case of contact with eyes, rinse eyes thoroughly with water
When using this product
Otc - Stop Use
- Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious conditions.
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
- Apply as needed into palm of hand and thoroughly spread on both hands, rub unitl dry.
- Supervise children under 6 years of age when using this product
Other Information
- Store between 15-30 (59-86 F)
- Avoid freezing and excessive heat above 40 C(104 F)
Inactive Ingredients
Deionized water, Triethanolamine, Carbomer, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate
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