BIOPURE- hand sanitizer spray liquid

Biopure by

Drug Labeling and Warnings

Biopure by is a Otc medication manufactured, distributed, or labeled by Quest USA Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

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

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

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

WHEN USING

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.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

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

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

● May discolor certain fabrics.

Inactive ingredients

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

Questions? call 718-975-2586

Package Label - Principal Display Panel

30 ml in 1 bottle

INGREDIENTS AND APPEARANCE

BIOPURE 
hand sanitizer spray liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-029
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	16 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
BLUE 1 (UNII: H3R47K3TBD)
ALPHA-ISOMETHYL IONONE (UNII: 9XP4LC555B)
PEONIFLORIN (UNII: 21AIQ4EV64)
TREHALOSE (UNII: B8WCK70T7I)
CITRUS AURANTIFOLIA (LIME) OIL (UNII: UZH29XGA8G)
CITRUS LIMON (LEMON) PEEL OIL (UNII: I9GRO824LL)
LINALOOL (UNII: D81QY6I88E)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
PROPANEDIOL (UNII: 5965N8W85T)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
YELLOW 5 (UNII: I753WB2F1M)
CITRAL (UNII: T7EU0O9VPP)
WATER (UNII: 059QF0KO0R)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
HEXYL CINNAMAL (UNII: 7X6O37OK2I)
GERANIOL (UNII: L837108USY)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERETH-26 (UNII: NNE56F2N14)
ACID RED 18 (UNII: Z525CBK9PG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78691-029-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/15/2025

Labeler - Quest USA Corp (079869689)