FDA.reportPublic FDA data

Rinse-Free Hand Sanitizer

Manufacturer
Ningbo Venus Cosmetic Co., Ltd.
Effective date
2020-11-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:33:56

Label at a glance#

ProductRinse-Free Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Do not shake before use. Pump gel onto your palm and massage your hands together until dry

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) Non staining, may discolor certain fabrics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

9HEADS-EAGLE Rinse-free Hand Sanitizer Gel has been formul ated to kill germs whilst helping to keep your hands smooth and soft.

DIRECTIONS

INDICATIONS & USAGE SECTION

Do not shake before use. Pump gel onto your palm and massage your hands together until dry

Warnings

WARNINGS SECTION

FLAMMABLE. Keep away from the source of fire and flame FOR EXTERNAL USE ONLY.

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

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

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

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

OTC - STOP USE SECTION

If skin irritation occurs, discontinue use.

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.

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

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)
  • Non staining, may discolor certain fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30303603605005006060700700

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
14341-005-012022-01-28C16284748780-1d6a99b39-ffa7-a426-e053-dadaa90af4c214341-005 Rinse-Free Hand Sanitizer
14341-005-022022-01-28C16284748780-1d6a99b39-ffa7-a426-e053-dadaa90af4c214341-005 Rinse-Free Hand Sanitizer
14341-005-032022-01-28C16284748780-1d6a99b39-ffa7-a426-e053-dadaa90af4c214341-005 Rinse-Free Hand Sanitizer
14341-005-042022-01-28C16284748780-1d6a99b39-ffa7-a426-e053-dadaa90af4c214341-005 Rinse-Free Hand Sanitizer
14341-005-052022-01-28C16284748780-1d6a99b39-ffa7-a426-e053-dadaa90af4c214341-005 Rinse-Free Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
14341-005-01Rinse-Free Hand Sanitizer30 mL in 1 BOTTLESPRAY304
14341-005-02Rinse-Free Hand Sanitizer60 mL in 1 BOTTLESPRAY604
14341-005-03Rinse-Free Hand Sanitizer360 mL in 1 BOTTLESPRAY3604
14341-005-04Rinse-Free Hand Sanitizer500 mL in 1 BOTTLESPRAY5004
14341-005-05Rinse-Free Hand Sanitizer700 mL in 1 BOTTLESPRAY7004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
14341-005RINSE-FREE HAND SANITIZER SPRAY [NINGBO VENUS COSMETIC CO., LTD.]4Legacy NDC, 5 package rows20201120_a39e5cdc-161c-1683-e053-2995a90a5593.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
14341-00514341-005-01, 14341-005-02, 14341-005-03, 14341-005-04, 14341-005-05

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
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
b47214af-ed47-2dca-e053-2995a90ae000a39e5cdc-161c-1683-e053-2995a90a55932020-11-19WarningsExact identifier
spl id: b47214af-ed47-2dca-e053-2995a90ae000
spl set id: a39e5cdc-161c-1683-e053-2995a90a5593

Reported adverse events (FAERS/openFDA)#

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