Active Ingredient
Ethyl Alcohol 75.05%
Hand Sanitizer
FDA Label NDC 73549-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fortress Expert Co., Ltd for the product Hand Sanitizer (NDC 73549-005). 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, 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
Uses
Helps reduce bacteria that potentially can cause disease
Helps prevent cross contamination by hand contact
Recommended for repeated use
Warnings
For external use only
Flammable, keep away from fire, heat,or flame
Do not use near eyes
In case of eye contact flush with water for 15 minutes
if irritation persists stop use of product and get medical attention
Keep out of reach of children.
In case of accidental ingestion seek medical attention or contact a poison control center immediately.
Directions
Wet hands thoroughly with product and and rub completely covering hands
Allow to dry without wiping
Children under the age of 6 should use with adult
supervision
Not recommended for infants
Inactive Ingredients
Water, PEG-40 Hydrogenated Castor Oil, Carbomer,
Fragrance (Parfum), Triethanolamine, Triisopropanolamine
Package Label - Principal Display Panel
3785 (3785.4)
946 (946.35)
2000 (2000)
60 (60)
* Please review the disclaimer below.
