b.pure Hand Sanitizer Spray, Watermelon Scented

Manufacturer: FOURSTAR GROUP USA, INC.
Effective date: 2024-07-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:16:04

Label at a glance#

Productb.pure Hand Sanitizer Watermelon Scented

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

hand sanitizer to help reduce bacteria on skin

Dosage and administration

Spray into hands and rub together briskly until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in or near the eyes In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation, excessive redness or rash develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray into hands and rub together briskly until dry.

Other information

SPL UNCLASSIFIED SECTION

Store below 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, fragrance, citrullus lanatus (watermelon) fruit extract

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041849	ethanol 70 % Topical Spray	PSN	1
1041849	ethanol 0.7 ML/ML Topical Spray	SCD	1
1041849	ethanol 70 % Topical Spray	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80684-124-00	b.pure Hand Sanitizer Watermelon Scented	10 mL in 1 BOTTLE	LIQUID	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80684-124	B.PURE HAND SANITIZER WATERMELON SCENTED (ALCOHOL) LIQUID [FOURSTAR GROUP USA, INC.]	1	Current NDC, 1 package rows	20240726_e0ed1b57-2d7e-4e63-96f5-dbbb2aef26df.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

b.pure Hand Sanitizer Watermelon Scented
ALCOHOL
WATER
GLYCERIN
WATERMELON

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80684-124	80684-124-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATERMELON	231473QB6R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b.pure Hand Sanitizer Watermelon Scented	ALCOHOL	FOURSTAR GROUP USA, INC.	e0ed1b57-2d7e-4e63-96f5-dbbb2aef26df	2024-07-12	Warnings	Exact identifier ndc (package): 80684-124-00 ndc (product): 80684-124 ndc11 (package): 80684012400 spl id: 1d0f7fd9-f14f-7e23-e063-6394a90a9c20 spl set id: e0ed1b57-2d7e-4e63-96f5-dbbb2aef26df

Reported adverse events (FAERS/openFDA)#

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