AshleyBelle Moisturizing Spray Hand Sanitizer Rainfall

Manufacturer: Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Effective date: 2025-06-03
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:02:05

Label at a glance#

ProductAshleyBelle Moisturizing Hand Sanitizer Rainfall

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Hand sanitiser to help reduce bacteria on the skin that could cause disease Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping For children under 6, do not use without adult supervision Not recommended for infants.

Storage and handling

Do not store above 110F (43C) May discolor certain fabrics or surfaces Harmful to wood finishes and plastics Keep away from heat and direct sunlight.

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 sanitiser to help reduce bacteria on the skin that could cause disease
Recommended for repeated use.

Warnings

WARNINGS SECTION

Highly Flammable. Keep away from fire or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

When using this product do not use 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

Stop use and ask a doctor if irritation or rash appears and lasts.

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
For children under 6, do not use without adult supervision
Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

Do not store above 110F (43C)
May discolor certain fabrics or surfaces
Harmful to wood finishes and plastics
Keep away from heat and direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua)

Glycerin

Aloe Barbadensis Leaf Juice

Fragrance

Denatonium Benzoate

Eucalyptus GlobulusLeaf oil

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

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
75742-040-01	AshleyBelle Moisturizing Hand Sanitizer Rainfall	29.5 mL in 1 BOTTLE, SPRAY	SPRAY	29.5		1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

AshleyBelle Moisturizing Hand Sanitizer Rainfall
Ethyl Alcohol 70%
WATER
ALOE BARBADENSIS LEAF JUICE
EUCALYPTUS GLOBULUS LEAF OIL
DENATONIUM BENZOATE
GLYCERIN
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75742-040	75742-040-01

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
ALOE BARBADENSIS LEAF JUICE	RUE8E6T4NB	IACT
EUCALYPTUS GLOBULUS LEAF OIL	2R04ONI662	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
GLYCERIN	PDC6A3C0OX	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
AshleyBelle Moisturizing Hand Sanitizer Rainfall	ETHYL ALCOHOL 70%	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	36a68ecb-3216-eeb2-e063-6294a90a5bba	2025-06-03	Warnings	Exact identifier ndc (package): 75742-040-01 ndc (product): 75742-040 ndc11 (package): 75742004001 spl id: 36a69442-2f28-949c-e063-6294a90aa00f spl set id: 36a68ecb-3216-eeb2-e063-6294a90a5bba

Reported adverse events (FAERS/openFDA)#

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