b pure Hydrating Hand Sanitizer Frosted Coconut Scented

Manufacturer: FOURSTAR GROUP USA, INC.
Effective date: 2024-06-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:22:36

Label at a glance#

Productb pure Hydrating Hand Sanitizer Frosted Coconut 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 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, benzyl salicylate, hexyl cinnamal, coumarin

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	1
582753	ethanol 0.7 ML/ML Topical Solution	SCD	1
582753	ethanol 70 % Topical Solution	SY	1
582753	ethyl alcohol 70 % Topical Solution	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80684-113-00	b pure Hydrating Hand Sanitizer Frosted Coconut Scented	30 mL in 1 BOTTLE	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80684-113	B PURE HYDRATING HAND SANITIZER FROSTED COCONUT SCENTED (ALCOHOL) LIQUID [FOURSTAR GROUP USA, INC.]	1	Current NDC, 1 package rows	20241004_dd57d7fa-deb3-4b02-a9cc-a39153afa049.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

b pure Hydrating Hand Sanitizer Frosted Coconut Scented
ALCOHOL
WATER
GLYCERIN
BENZYL SALICYLATE
.ALPHA.-HEXYLCINNAMALDEHYDE
COUMARIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
80684-113	80684-113-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
BENZYL SALICYLATE	WAO5MNK9TU	IACT
.ALPHA.-HEXYLCINNAMALDEHYDE	7X6O37OK2I	IACT
COUMARIN	A4VZ22K1WT	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 Hydrating Hand Sanitizer Frosted Coconut Scented	ALCOHOL	FOURSTAR GROUP USA, INC.	dd57d7fa-deb3-4b02-a9cc-a39153afa049	2024-06-24	Warnings	Exact identifier ndc (package): 80684-113-00 ndc (product): 80684-113 ndc11 (package): 80684011300 spl id: 1baa9c60-b015-72fe-e063-6394a90a254f spl set id: dd57d7fa-deb3-4b02-a9cc-a39153afa049

Reported adverse events (FAERS/openFDA)#

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