Active Ingredient
Ethyl alcohol 62%
Antiseptic Hand Sanitizer
FDA Label NDC 65055-600
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Jaloma S.a. De C.v. for the product Antiseptic Hand Sanitizer (NDC 65055-600). 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, purpose, use, warnings, do not use, 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
Use
For hand washing to decrease bacteria on the skin
Warnings
For external use only
Flammable, keep away from fire or flame.
Do Not Use
in the eyes
Stop Use And Ask A Doctor If
- irritation and redness develop
- condition persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
wet hands thoroughly with product and allow to dry without wiping
Other Information
- do not store above 110°F (43°C)
- may discolor certain fabrics, or may harm some wood finishes and plastics
Inactive Ingredients
Water, glycerin, fragrance, tocopherol acetate, carbomer and triethanolamine.
Questions Or Comments?
+1 818 763 8698
Package Labeling: (65055-600-00)
Label2 (Label2)
Label (Label)
Package Labeling: (65055-600-01)
Label3 (Label3)
Label4 (Label4)
Package Labeling: (65055-600-02)
Label5 (Label5)
Label6 (Label6)
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