Active Ingredient(S)
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 51706-913
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Landy International for the product Hand Sanitizer (NDC 51706-913). 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, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
helps eliminate bacteria on hands
Warnings
For external use only.
Flammable, Keep away from heat or flame,
Do not use
On children less than 2 months of age. on open skin wounds
When using this product keep out of eyes, ear, and mouth.
In case of contact with eve, rinse eyes thouroughly with water
Stop use and ask a doctor if irritation or rash occurs,
These may be a sign of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. except under adult supervision.
If swallowed, get medical help or contact a poison control center right away.
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.
Inactive Ingredients
Acrylates(C10-30 acrylate crosspolymer, Ascorbyl palmitate, Blue 1 (CI42090),
Celluulose, Coumarin, Fagrance (Parfum), Glycein, Hydroxypropvl methylcellulose, Jojoba
Esters, lactose, Limonene, Linalool, Red 33( CI17200), Tocopheryl acetate,
Triethanolamine, Ultramarines (CI77007), Water(Aqua).
Package Label - Principal Display Panel
* Please review the disclaimer below.
