Active Ingredient
Ethyl Alcohol 62%
Anti Bacterial Hand Sanitizer
FDA Label NDC 49852-012
9 label sections · Submitted to the FDA by Tri-coastal Design Company Inc. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tri-coastal Design Company Inc. for the product Anti Bacterial Hand Sanitizer (NDC 49852-012). 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, uses, warnings, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
• For handwashing to decrease bacteria on the skin
Warnings
• For external use only
• Flammable, keep away from fire and flame
Does not contain grain alcohol. Do not drink. If taken internally will produce serious gastric disturbances
Avoid eyes and mucous membranes
In case of contact, rinse area throoughly with water
Keep Out Of Reach Of Children
If swallowed contact a doctor or Poison Control Center immediately
Directions
Rub dime sized amount between hands until dry
Other Information
Store below 105°F
May discolor some fabrics
Inactive Ingredients
Benzophenone-4, Carbomer, Fragrance, FD&C Blue 1, Glycerin, PEG-40 Hydrogenated Castor Oil, Propylene Glycol, Tocopherol, Jojoba Oil, Triethanolamine, Water(Aqua)
Package Label
Package Label (Bluhndsntzr)
* Please review the disclaimer below.
