Active Ingredient
Ethyl Alcohol 80% v/v
Adventure Hand Sanitizer - Fragrance 80% Spray
FDA Label NDC 77371-124
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nicety Solutions Llc for the product Adventure Hand Sanitizer - Fragrance 80% (NDC 77371-124). 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, keep out of reach of children, stop use and ask a doctor if, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
For hand sanitizing to decrease bacteria on skin.
Warnings
For external use only
Flammable, keep away from fire and flame
Do Not Use
in the eyes
Keep Out Of Reach Of Children
If swallowed, get medical help or contact an Poison Control Center right away.
Stop Use And Ask A Doctor If
redness or irritation develops and persists for more than 72 hours
Directions
Spray hands thoroughly. Rub hands together until dry.
Inactive Ingredients
Water, Propanediol, Aloe Vera Powder, Panthenol, Hydroxyethylcellulose
Label
Adventure Hand Santitizer
By the makers of Shower Pouch
Remove odors
Kills germs on the go
1.3 fl oz [38 ml]
Front (Fragranced Front All)
* Please review the disclaimer below.
