BODY PRESCRIPTIONS Eucalyptus ANTIBACTERIAL HAND SANITIZER

Manufacturer: ENCHANTE ACCESSORIES INC. | Xiamen Afgamarine Biotechnology Co., Ltd.
Effective date: 2021-03-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:39:15

Label at a glance#

ProductBODY PRESCRIPTIONS Eucalyptus ANTIBACTERIAL HAND SANITIZER

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

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

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat: 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

■ To decrease bacteria on the skin that could cause disease
■Recommended for repeated use

WARNINGS

WARNINGS SECTION

For external use only

Flammable. Keep away from heat and flame

OTC - WHEN USING SECTION

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water

Avoid contact with broken skin

Do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

For children under 6, use only under adult supervision

Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Fragrance, Blue 1, Yellow 5

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286295	ethanol 75 % Topical Spray	PSN	1
2286295	ethanol 0.75 ML/ML Topical Spray	SCD	1
2286295	ethanol 75 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50563-418-01	2022-07-29	C162847	48780-1	e4f33bdf-a771-d8a0-e053-dadaa90a6e4e	50563-418/JAS21AS5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50563-418-01	BODY PRESCRIPTIONS Eucalyptus ANTIBACTERIAL HAND SANITIZER	100 mL in 1 BOTTLE	SPRAY	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50563-418	BODY PRESCRIPTIONS EUCALYPTUS ANTIBACTERIAL HAND SANITIZER (ETHYL ALCOHOL) SPRAY [ENCHANTE ACCESSORIES INC.]	1	Legacy NDC, 1 package rows	20210327_f4127af6-1381-4e2d-be5c-bb24a49e2887.zip

Products#

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

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

BODY PRESCRIPTIONS Eucalyptus ANTIBACTERIAL HAND SANITIZER
Ethyl Alcohol
WATER
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50563-418	50563-418-01

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
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	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
be73555f-88cf-33bb-e053-2995a90a5796			f4127af6-1381-4e2d-be5c-bb24a49e2887	2021-03-26	Warnings	Exact identifier spl id: be73555f-88cf-33bb-e053-2995a90a5796 spl set id: f4127af6-1381-4e2d-be5c-bb24a49e2887

Reported adverse events (FAERS/openFDA)#

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