Active Ingedient
Ethanol (ethyl alcohol) (70%)
Medicare Hand Sanitizer (50ml)
FDA Label NDC 73786-103
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by B&d Life Health Co., Ltd. for the product Medicare Hand Sanitizer (50ml) (NDC 73786-103). 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 ingedient, purpose, uses, warnings, keep out of reach of children, directions, inactive ingredients, medicare hand sanitizer (50ml), and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
Hand sanitizer for decreasing bacteria on skin
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.
Stop use and ask a doctor if irritation or redness develops and the condition persists for more than 72 hours.
If pregnant or breast-feeding, ask a health professional before use
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
Apply the adequate amount on hands
Inactive Ingredients
Purified water, Glycerin, L-menthol, Carbomer, Aminomethyl Propanol, Aloe extract
* Please review the disclaimer below.
