FDA Label for Hand Sanitizer
View Indications, Usage & Precautions
Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product Leidos Biomedical Researh, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Hand Sanitizer Labels (Front Label And Drug Facts Label)
Alcohol 80 % v/v
Otc - Purpose
Antiseptic
Indications & Usage
Health care personnel hand rub to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - Do Not Use
- In children less than 2 months of age
- On open skin wounds
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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.
Dosage & Administration
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 Safety Information
Other Information:
Store between 15-30c (59-86F)
Avoid freezing and excessive heat above 40 C (104F)
Inactive Ingredient
Inactive ingredients glycerin, hydrogen peroxide, purified water USP
Otc - Active Ingredient
450 mL NDC 74167-8001-1
Package Label.Principal Display Panel
450 mL NDC: 74167-8001-1
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