BEAUTANIQ BEAUTY HAND SANITIZER

Manufacturer: CROP BEAUTY GROUP INC. | Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date: 2023-10-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:57:54

Label at a glance#

ProductBEAUTANIQ BEAUTY HAND SANITIZER

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic.

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available.

Warnings

WARNINGS SECTION

Flammable, keep away from fire and flames

For external use only

When using this product

OTC - WHEN USING SECTION

do not get into eyes.
if contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop.

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

wet hands thoroughly with product and allow to dry without wiping.

Other information

SPL UNCLASSIFIED SECTION

Store below 105 °F.
May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Aloe Barbadensis Extract,Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020364	ethanol 62 % Topical Spray	PSN	2
1020364	ethanol 0.62 ML/ML Topical Spray	SCD	2
1020364	ethanol 62 % Topical Spray	SY	2
1020364	ethyl alcohol 62 % Topical Spray	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78768-001-50	BEAUTANIQ BEAUTY HAND SANITIZER	50 mL in 1 BOTTLE	SPRAY	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78768-001	BEAUTANIQ BEAUTY HAND SANITIZER (ALCOHOL) SPRAY [CROP BEAUTY GROUP INC.]	2	Current NDC, Legacy NDC, 1 package rows	20231026_e410c167-01a2-4908-a9a7-d1c5bdfe8de4.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

BEAUTANIQ BEAUTY HAND SANITIZER
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78768-001	78768-001-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	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
BEAUTANIQ BEAUTY HAND SANITIZER	ALCOHOL	CROP BEAUTY GROUP INC.	e410c167-01a2-4908-a9a7-d1c5bdfe8de4	2023-10-26	Warnings	Exact identifier ndc (package): 78768-001-50 ndc (product): 78768-001 ndc11 (package): 78768000150 spl id: 0897ac32-872e-c027-e063-6294a90a3985 spl set id: e410c167-01a2-4908-a9a7-d1c5bdfe8de4

Reported adverse events (FAERS/openFDA)#

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