BIOPURE HAND SANITIZER SPRAY-LAVENDER

Manufacturer
Quest USA Corp
Effective date
2025-07-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:07:48

Label at a glance#

ProductBiopure
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Directions ●Spray enough product in your palm to thoroughly cover your hands. ●Rub hands together briskly until dry. Recommended for repeated use. ●Children under 6 years of age should be supervised by an adult when using this product.

Storage and handling

● Protect the product in this container from excessive heat and direct sun. ● Store below 104°F (40°C). ● May discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Hand sanitizer to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

Stop use and ask doctor
if irritation and rash occurs. These may be signs of serious condition.

OTC - WHEN USING SECTION

When using this product
keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Avoid contact with broken skin.

OTC - STOP USE SECTION

Stop use and ask doctorif irritation and rash occurs. These may be signs of serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
●Spray enough product in your palm to thoroughly cover your hands.

●Rub hands together briskly until dry. Recommended for repeated use.

●Children under 6 years of age should be supervised by an adult when using this product.

Other information

STORAGE AND HANDLING SECTION

● Protect the product in this container from excessive heat and direct sun.
● Store below 104°F (40°C).

● May discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance, Glycereth-26,Hexyl Cinnamal, Citrus Aurantifolia (Lime) Oil, Propanediol, Linalool,Alpha-lsomethyl lonone,Citral, Citronellol, Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Peel Oil,Trehalose, Geraniol,Scutellaria Baicalensis Root Extract, Peoniflorin,Leuconostoc/ Radish Root Ferment Filtrate, Yellow 5, Blue 1, Acid Red 18

Questions

OTC - QUESTIONS SECTION

Questions? call 718-975-2586

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 ml in 1 bottle

Hand Sanitizer Spray Label2Hand Sanitizer Spray Label2

Hand Sanitizer Spray LabelHand Sanitizer Spray Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78691-028-01Biopure30 mL in 1 BOTTLE, SPRAYLIQUID302

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78691-02878691-028-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BiopureHAND SANITIZER SPRAYQuest USA Corp3249f563-7968-e512-e063-6394a90aad522025-07-18WarningsExact identifier
ndc (package): 78691-028-01
ndc (product): 78691-028
ndc11 (package): 78691002801
spl id: 3a3c0aa0-7504-7ef0-e063-6294a90a9f94
spl set id: 3249f563-7968-e512-e063-6394a90aad52

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.