Otc - Active Ingredient
Active Ingredient Purpose
Ethyl Alcohol (62 percent) Antiseptic
Antibacterial Hand Sanitizer Spray
FDA Label NDC 49701-2000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Webb Company for the product Antibacterial Hand Sanitizer Spray (NDC 49701-2000). 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 otc - active ingredient, warnings, dosage & administration, inactive ingredient, description, 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
Warnings
Warnings Flammable.
Keep away from open flame.
Keep out of reach of children.
Dosage & Administration
Directions: Spray small amount in your palm and briskly rub hands together until dry.
Inactive Ingredient
Inactive Ingredients
water, silicone oil (water soluble) vitamin E, Aloe vera oil, fragrance
Description
(0.34 oz) Made in China
Package Label.Principal Display Panel
Handsanitizer10ml (10ml)
* Please review the disclaimer below.
