Hand Sanitizer

Manufacturer
GUANGZHOU CANYON BIOTECHNOLOGY CO.,LTD
Effective date
2020-04-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:06

Label at a glance#

ProductHand Sanitizer
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

do not store above 105"F may discolor fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer 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

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

When using this product a avoid getting into the eyes. in case of eye contact immediately flush eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops.conditions persist for more than 72 hours m redness is present.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

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.

Other information

STORAGE AND HANDLING SECTION

  • do not store above 105"F
  • may discolor fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, carbomer sodium hyrdoxide, aloe yohjyu matsu ekisu.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250ml250ml500ml500ml

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75675-005-012022-01-28C16284748780-1d6a99b39-7025-a426-e053-dadaa90af4c2a38cfe45-7a24-1d78-e053-2995a90ae8b9
75675-005-022022-01-28C16284748780-1d6a99b39-7025-a426-e053-dadaa90af4c2a38cfe45-7a24-1d78-e053-2995a90ae8b9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75675-005-01Hand Sanitizer250 mL in 1 BOTTLELIQUID2501
75675-005-02Hand Sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75675-005HAND SANITIZER LIQUID [GUANGZHOU CANYON BIOTECHNOLOGY CO.,LTD]1Legacy NDC, 2 package rows20200421_a38cfe45-7a24-1d78-e053-2995a90ae8b9.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
75675-00575675-005-01, 75675-005-02

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
a38cfc83-3d8a-edc0-e053-2995a90aa192a38cfe45-7a24-1d78-e053-2995a90ae8b92020-04-18WarningsExact identifier
spl id: a38cfc83-3d8a-edc0-e053-2995a90aa192
spl set id: a38cfe45-7a24-1d78-e053-2995a90ae8b9

Reported adverse events (FAERS/openFDA)#

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