FDA.reportPublic FDA data

75% Alcohol Wipes

Manufacturer
Anhui Hanbon Daily Chemical Co., Ltd.
Effective date
2022-01-23
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:47:41

Label at a glance#

Product75% Alcohol Wipes
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wipe the surface of the skin and let it air dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store at room temperature. Keep pouch tightly closed and stored at room temperature. Hold away from face when opening.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For hand sanitizing that helps reduce bacteria on the skin.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, Keep away from fire or flame, heat, spark, electrical.

Do not use

OTC - DO NOT USE SECTION

  • On 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.

OTC - STOP USE SECTION

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

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

  • Wipe the surface of the skin and let it air dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store at room temperature.
  • Keep pouch tightly closed and stored at room temperature.
  • Hold away from face when opening.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerol, Propane -1,2-diol, Benzalkonium Chloride, Aloe Vera Extract, Cetylpyridinium Chloride, Didecyldimethylammonium Chloride, Tea Tree Oil, Matricaria Recutita Extract, Quaternary, Citric Acid.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10 PATCH in 1 PACKET NDC: 40562-009-01 10pcs label10pcs label

50 PATCH in 1 PACKET NDC: 40562-009-02

40 PATCH in 1 PACKET NDC: 40562-009-03

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40562-009-012024-01-30C16284748780-11030e365-34a4-111a-e063-dadaa90a10e2Hanbon 75% Alcohol Wipes Update label.jpg
40562-009-022024-01-30C16284748780-11030e365-34a4-111a-e063-dadaa90a10e2Hanbon 75% Alcohol Wipes Update label.jpg
40562-009-032024-01-30C16284748780-11030e365-34a4-111a-e063-dadaa90a10e2Hanbon 75% Alcohol Wipes Update label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40562-009-0175% Alcohol Wipes10 in 1 PACKETCLOTH105
40562-009-0175% Alcohol Wipes4 mL in 1 PATCHCLOTH45
40562-009-0275% Alcohol Wipes4 mL in 1 PATCHCLOTH45
40562-009-0275% Alcohol Wipes50 in 1 PACKETCLOTH505
40562-009-0375% Alcohol Wipes4 mL in 1 PATCHCLOTH45
40562-009-0375% Alcohol Wipes40 in 1 PACKETCLOTH405

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40562-00975% ALCOHOL WIPES (ALCOHOL WIPES) CLOTH [ANHUI HANBON DAILY CHEMICAL CO., LTD.]5Legacy NDC, 6 package rows20220128_a837664e-cd08-67af-e053-2995a90ad89a.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
40562-00940562-009-01, 40562-009-02, 40562-009-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
CETYLPYRIDINIUM CHLORIDE ANHYDROUS6BR7T22E2SIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
CHAMOMILEFGL3685T2XIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)G258TFN61XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TEA TREE OILVIF565UC2GIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT

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
d63a2454-b6c7-98de-e053-2995a90a3e7aa837664e-cd08-67af-e053-2995a90ad89a2022-01-23WarningsExact identifier
spl id: d63a2454-b6c7-98de-e053-2995a90a3e7a
spl set id: a837664e-cd08-67af-e053-2995a90ad89a

Reported adverse events (FAERS/openFDA)#

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