B-Pure Moisturizing Hand Sanitizer, Vanilla Creme Scented

Manufacturer: Fourstar Group USA, Inc.
Effective date: 2026-04-28
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:55:14

Label at a glance#

ProductB-Pure Moisturizing Hand Sanitizer Vanilla Creme Scented

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

hand sanitizer to help reduce bacteria on skin

Dosage and administration

Spray product in hands and rub together.

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 product in hands and rub together.

Other information

SPL UNCLASSIFIED SECTION

Store below 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, fragrance, glycerin, yellow 5, red 4

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1041849	ethanol 70 % Topical Spray	PSN	2
1041849	ethanol 0.7 ML/ML Topical Spray	SCD	2
1041849	ethanol 70 % Topical Spray	SY	2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80684-183-01	B-Pure Moisturizing Hand Sanitizer Vanilla Creme Scented	34 mL in 1 BOTTLE	LIQUID	34		2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

B-Pure Moisturizing Hand Sanitizer Vanilla Creme Scented
ALCOHOL
WATER
GLYCERIN
FD&C YELLOW NO. 5
FD&C RED NO. 4

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80684-183	80684-183-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C RED NO. 4	X3W0AM1JLX	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
1	2025-12-02	monthly-update	2026-06-03 17:45:17

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 Moisturizing Hand Sanitizer Vanilla Creme Scented	ALCOHOL	Fourstar Group USA, Inc.	13faded0-7953-4d86-b952-e4bcf4ba53cc	2026-04-28	Warnings	Exact identifier ndc (package): 80684-183-01 ndc (product): 80684-183 ndc11 (package): 80684018301 spl id: 508680d5-84eb-7717-e063-6394a90a3576 spl set id: 13faded0-7953-4d86-b952-e4bcf4ba53cc

Reported adverse events (FAERS/openFDA)#

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