Eucalyptus Hand Wipes

Manufacturer
Dr. Brite
Effective date
2022-02-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:48:18

Label at a glance#

ProductEucalyptus Hand Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Storage and handling

Store at room temperature, do not store above 102°F. DO not keep in hot car. Do not store near heat or open flame. Please recycle when available.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v.

OTC - PURPOSE SECTION

Antiseptic

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purifies Water, Hydrogen Peroxide, Peppermint Leaf Oil, Eucalyptus Leaf Oil, Lauric Acid, Citric Acid.

DOSAGE & ADMINISTRATION SECTION

Directions For Use

INDICATIONS & USAGE SECTION

Open the lid and peel back the seal. When finished, close to retain moisture.

Remove a wipe, wipe thoroughly until clean. Larger messes may require two wipes.

Allow to air dry. No rinsing or drying is required, even on food prep areas.

NOT SUITABLE FOR: Porous materials, leather, silk clothing or stained woods.

Storage & Disposal

STORAGE AND HANDLING SECTION

Store at room temperature, do not store above 102°F. DO not keep in hot car. Do not store near heat or open flame. Please recycle when available.

Caution

WARNINGS SECTION

Caution

  • Flammable. Keep away from heat or flame.
  • Keep out of reach of children and pets.
  • May cause eye irritation.
  • Do not use as a diaper wipe.

Precautions

  • Avoid contact with eyes.
  • Avoid contact with clothing.
  • May cause staining or discoloration.
  • Always perform a spot test prior to use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

First-Aid

USER SAFETY WARNINGS SECTION

IF SWALLOWED: Get medical help or contact a Poison Control Center right away at 1-800-222-1222.

IF IN EYES: Rinse cautiously with water for several minutes. Seek medical attention if irritation persists. If skin irritation or redness occurs, discontinue use.

For Questions or Concerns

OTC - QUESTIONS SECTION

For questions or concerns, please call 949-748-7873

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74110-002-012024-01-30C16284748780-11030e365-5ddb-111a-e063-dadaa90a10e2Dr. Brite Eucalyptus Hand Wipes
74110-002-022024-01-30C16284748780-11030e365-5ddb-111a-e063-dadaa90a10e2Dr. Brite Eucalyptus Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74110-002-01Eucalyptus Hand Wipes54 in 1 BAGCLOTH541
74110-002-01Eucalyptus Hand Wipes5.4 mL in 1 PATCHCLOTH5.41
74110-002-02Eucalyptus Hand Wipes5.4 mL in 1 PATCHCLOTH5.41
74110-002-02Eucalyptus Hand Wipes10 in 1 POUCHCLOTH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74110-002EUCALYPTUS HAND WIPES (ISOPROPYL ALCOHOL) CLOTH [DR. BRITE]1Legacy NDC, 4 package rows20220217_d824fb93-a2b9-7712-e053-2995a90a2a9f.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74110-00274110-002-01, 74110-002-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
d8251c7a-bf3f-2d3b-e053-2995a90a2bc2d824fb93-a2b9-7712-e053-2995a90a2a9f2022-02-16WarningsExact identifier
spl id: d8251c7a-bf3f-2d3b-e053-2995a90a2bc2
spl set id: d824fb93-a2b9-7712-e053-2995a90a2a9f

Reported adverse events (FAERS/openFDA)#

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