Alcohol Hand Rub

Manufacturer
Zhejiang RIFESHOW Cosmetics Co., Ltd.
Effective date
2022-03-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:48:40

Label at a glance#

ProductBANITORE Alcohol Hand Rub
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30℃(59-86℉). Avoid freezing and excessive heat above 40℃(104℉).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • Hand Rub to help reduce bacteria that potentially can cause disease.
  • For use when soap and water are not available.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable. Keep away from heat or flame.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age.
  • on open skin wounds.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30℃(59-86℉).
  • Avoid freezing and excessive heat above 40℃(104℉).

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, glycerin, hydrogen peroxide.

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes througthly with water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500ml label500ml label 500mL NDC: 56084-031-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN3
1039339ethanol 0.8 ML/ML Topical SolutionSCD3
1039339ethanol 80 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56084-031-012023-07-28C16284748780-10191ceaa-70ec-198a-e063-dbdaa90aec3eZhejiang RIFESHOW Cosmetics Co., Ltd. Alcohol Hand Rub 500ml 56084-029-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56084-031-01BANITORE Alcohol Hand Rub500 mL in 1 BOTTLELIQUID5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56084-031BANITORE ALCOHOL HAND RUB (ALCOHOL) LIQUID [ZHEJIANG RIFESHOW COSMETICS CO., LTD.]3Legacy NDC, 1 package rows20220310_d978d0af-8a86-0e97-e053-2a95a90a63e7.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56084-03156084-031-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
d9c807a5-c21a-e044-e053-2995a90a4770d978d0af-8a86-0e97-e053-2a95a90a63e72022-03-09WarningsExact identifier
spl id: d9c807a5-c21a-e044-e053-2995a90a4770
spl set id: d978d0af-8a86-0e97-e053-2a95a90a63e7

Reported adverse events (FAERS/openFDA)#

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