FDA.reportPublic FDA data

Aulani Disney Resort and Spa Hawaii Alcohol Wet Wipe

Manufacturer
MING FAI ENTERPRISE INTERNATIONAL CO., LTD
Effective date
2024-03-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:07:23

Label at a glance#

ProductAulani Disney Resort and Spa Hawaii Alcohol Wet Wipe
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

to help reduce bacteria on the skin.

Dosage and administration

Appyl to hands or skin. No rinsing required. Discard after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72% (v/v)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

  • For external use only.
  • Do not dispose of wipes in flush toilets. 
  • Keep away from fire or flame.

Flammable

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes.
  • If contact occurs, rinse thoroughly with water.

Stop using and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Appyl to hands or skin. No rinsing required. Discard after use.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Polyquaternium-37, Melaleuca Alternifolia Leaf Oil (tea tree oil)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74548-016AULANI DISNEY RESORT AND SPA HAWAII ALCOHOL WET WIPE (ALCOHOL) CLOTH [MING FAI ENTERPRISE INTERNATIONAL CO., LTD]4Legacy NDC20240328_e6d11049-d5d9-4a38-ae11-04cac133bb7d.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
74548-01674548-016-01

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TEA TREE OILVIF565UC2GIACT
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
14958fa2-ba93-cc9d-e063-6294a90ad22ce6d11049-d5d9-4a38-ae11-04cac133bb7d2024-03-26WarningsExact identifier
spl id: 14958fa2-ba93-cc9d-e063-6294a90ad22c
spl set id: e6d11049-d5d9-4a38-ae11-04cac133bb7d

Reported adverse events (FAERS/openFDA)#

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