AllcareU Disposable HAND SANITIZER

Manufacturer
JIANGSU AllCARE BIOTECH PHARMACEUTICAL CO., LTD
Effective date
2020-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:09

Label at a glance#

ProductAllcareU Disposable HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and rub until 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(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% 

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To reduce bacteria on the skin that could cause disease

Recommended for repeated use

Use anywhere without water

Warnings

WARNINGS SECTION

For external use only -hands

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

Discontinue if skin becomes irritated and ask a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingest, seek professional assistance or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and rub until 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, glycerin, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, triethanolamine, fragrance, PANTHENOL, LONICERA JAPONICA(HONEYSUCKLE) FLOWER EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
884783ethanol 65 % Topical SolutionPSN1
884783ethanol 0.65 ML/ML Topical SolutionSCD1
884783ethanol 65 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78988-001-01AllcareU Disposable HAND SANITIZER89 mL in 1 BOTTLESOLUTION891
78988-001-02AllcareU Disposable HAND SANITIZER354 mL in 1 BOTTLESOLUTION3541
78988-001-03AllcareU Disposable HAND SANITIZER500 mL in 1 BOTTLESOLUTION5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78988-001ALLCAREU DISPOSABLE HAND SANITIZER (ALCOHOL) SOLUTION [JIANGSU ALLCARE BIOTECH PHARMACEUTICAL CO., LTD]1Legacy NDC, 3 package rows20200714_4359be70-e8d4-4505-9dd1-829e2c24b648.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78988-00178988-001-01, 78988-001-02, 78988-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
aa58eb89-2a2c-79ea-e053-2a95a90ae3ff4359be70-e8d4-4505-9dd1-829e2c24b6482020-07-13WarningsExact identifier
spl id: aa58eb89-2a2c-79ea-e053-2a95a90ae3ff
spl set id: 4359be70-e8d4-4505-9dd1-829e2c24b648

Reported adverse events (FAERS/openFDA)#

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