eco harbor HAND SANITIZING MIST EUCALYPTUS MINT

Manufacturer
ENCHANTE ACCESSORIES INC. | Xiamen Wally Bath Manufacture Co., Ltd
Effective date
2023-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:30:31

Label at a glance#

Producteco harbor HAND SANITIZING MIST EUCALYPTUS MINT
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Spray into palm and rub hands together Allow to dry without wiping

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

Ethyl Alcohol: 75% (W/W)

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

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.

For children under 6 years of age, use only under adult supervision

If swallowed, get medical help or contact a poison control center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Spray into palm and rub hands together

Allow to dry without wiping

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, Glycerin, PEG-40 Hydrogenated Castor Oil, Fragrance, Aloe Barbadensis Leaf Extract, Eucalyptus Globulus Leaf Extract, Mentha Arvensis Extract, Yellow 5, Blue 1.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50563-471-012025-03-18C16284748780-11030e365-050c-111a-e063-dadaa90a10e250563-471/ PS3HSM01
50563-471-012024-07-30C16284748780-11030e365-050c-111a-e063-dadaa90a10e250563-471/ PS3HSM01
50563-471-012024-01-30C16284748780-11030e365-050c-111a-e063-dadaa90a10e250563-471/ PS3HSM01

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50563-47150563-471-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
30a506e8-8eb6-275d-e063-6294a90a07aaf083fbb5-9e40-43f8-9fc0-60e011babdab2025-03-18WarningsExact identifier
spl set id: f083fbb5-9e40-43f8-9fc0-60e011babdab

Reported adverse events (FAERS/openFDA)#

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