FDA.reportPublic FDA data

Alcohol Wipes

Manufacturer
JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Effective date
2017-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:39

Label at a glance#

ProductAlcohol Wipes
Active ingredientAlcohol
Label structure8 sections

Indications and uses

To decrease bacterial on the skin that could cause disease. Clean and refresh hands and face.

Dosage and administration

Wet hands and face thoroughly with product and allow to dry without wiping For children under 6, use only under adult supervision. Not recommended for infants. Other Information: do not store above 105 F. may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 31% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

  • To decrease bacterial on the skin that could cause disease.
  • Clean and refresh hands and face.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

  • Flammable, keep away from heat and flame.
  • When using this product, keep out of eyes. In case of eye contact, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.
  • Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Wet hands and face thoroughly with product and allow to dry without wiping
  • For children under 6, use only under adult supervision.
  • Not recommended for infants.

Other Information:

  • do not store above 105 F.
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

alcohol, water, acetone, phenylphenol, triethanolamine, poly methacrylate, essence

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel – Case Label

Alcohol WIPES

Principal Display Panel
Principal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1663812ethanol 31 % Medicated PadPSN1
1663812ethanol 0.31 ML/ML Medicated PadSCD1
1663812ethanol 31 % Medicated PadSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71734-202-01Alcohol Wipes3.6 mL in 1 PACKAGECLOTH3.61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71734-202ALCOHOL WIPES (ALCOHOL) CLOTH [JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.]1Current NDC, Legacy NDC, 1 package rows20171010_14dbe9dc-2504-4181-9565-5fa7c1a9c377.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71734-20271734-202-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Aloe Vera LeafZY81Z83H0XIACT
Propylene Glycol6DC9Q167V3IACT
Water059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT

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
Alcohol WipesALCOHOLJIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.14dbe9dc-2504-4181-9565-5fa7c1a9c3772017-10-09WarningsExact identifier
ndc (package): 71734-202-01
ndc (product): 71734-202
ndc11 (package): 71734020201
spl id: 5fc8221b-7d69-45b2-a720-f12ea913f840
spl set id: 14dbe9dc-2504-4181-9565-5fa7c1a9c377

Reported adverse events (FAERS/openFDA)#

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