50 Pack Alcohol Hand Wipes-Fresh Scent

Manufacturer
Hero Brands, Inc. | Zhuji Jianhe Paper Co., Ltd
Effective date
2020-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:30:05

Label at a glance#

Product50 Pack Alcohol Hand Wipes-Fresh Scent
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under 6 years of age should be supervised when using product.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 75% v/v. Purpose: Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

  • For external use only.
  • Keep away from fire or flame

When using

OTC - WHEN USING SECTION

When using this product keep out of eyes. If contact with eyes occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under 6 years of age should be supervised when using product.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Fragrance.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 CLOTH IN 1 CONISTER NDC: 90114-501-02

50 cloth label50 cloth label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90114-501-022022-01-28C16284748780-1d6a99b39-e2a9-a426-e053-dadaa90af4c290114-501-02 50 Pack Alcohol Hand Wipes-Fresh Scent jianhe 20200923 71563-051

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90114-501-0250 Pack Alcohol Hand Wipes-Fresh Scent4 mL in 1 PATCHCLOTH41
90114-501-0250 Pack Alcohol Hand Wipes-Fresh Scent50 in 1 PACKAGECLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90114-50150 PACK ALCOHOL HAND WIPES-FRESH SCENT CLOTH [HERO BRANDS, INC.]1Legacy NDC, 2 package rows20200924_affe46cc-3f7c-aeae-e053-2a95a90a3404.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90114-50190114-501-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
affe46cc-3f7d-aeae-e053-2a95a90a3404affe46cc-3f7c-aeae-e053-2a95a90a34042020-09-23WarningsExact identifier
spl id: affe46cc-3f7d-aeae-e053-2a95a90a3404
spl set id: affe46cc-3f7c-aeae-e053-2a95a90a3404

Reported adverse events (FAERS/openFDA)#

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