B-PURE HAND SANITIZER CHERRY SCENTED- alcohol liquid

B-Pure Hand Sanitizer Cherry Scented by

Drug Labeling and Warnings

B-Pure Hand Sanitizer Cherry Scented by is a Otc medication manufactured, distributed, or labeled by Fourstar Group USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

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, prunus avium (sweet cherry) fruit extract, tetramethyl acetyloctahydronaphthalenes, vanillin, hexamethylindanopyran, coumarin, benzaldehyde, limonene, trimethylcyclopentenyl methylisopentenol, red 33, red 4

Package Labeling: 10ml

Package Labeling: 59ml

INGREDIENTS AND APPEARANCE

B-PURE HAND SANITIZER CHERRY SCENTED 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80684-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SWEET CHERRY (UNII: 93T4562ZI3)
TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES (UNII: 2JU6ZH6GRE)
VANILLIN (UNII: CHI530446X)
HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)
COUMARIN (UNII: A4VZ22K1WT)
BENZALDEHYDE (UNII: TA269SD04T)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80684-203-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/12/2026
2	NDC: 80684-203-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/12/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505(a)(3)	03/12/2026

Labeler - Fourstar Group USA, Inc. (140099503)

Registrant - Fourstar Group USA, Inc. (140099503)