B-pure Hand Sanitizer Vanilla Honey Scented Liquid
FDA Label NDC 80684-205
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fourstar Group Usa, Inc. for the product B-pure Hand Sanitizer Vanilla Honey Scented (NDC 80684-205). 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 drug facts, active ingredient, purpose, uses, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol, 70% v/v
Purpose
Antimicrobial
Uses
hand sanitizer to help reduce bacteria on skin
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
in or near the eyes In case of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation, excessive redness or rash develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Spray into hands and rub together briskly until dry.
Other Information
Store below 110°F (43°C)
Inactive Ingredients
water, fragrance, glycerin, honey extract, hexamethylindanopyran, linalool, linalyl acetate, tetramethyl acetyloctahydronaphthalenes, benzyl salicylate, alpha-isomethyl ionone, citronellol, dimethyl phenethyl acetate, coumarin, citrus limon peel oil, vanillin, terpineol, limonene, juniperus virginiana oil, geranyl acetate, hydroxycitronellal, pinene, yellow 5, red 4
Package Labeling: 10Ml
Bottle3 (Bottle3)
Package Labeling: 59Ml
Bottle03 (Bottle03)
* Please review the disclaimer below.
