FDA.reportPublic FDA data

Murchison-Hume Wellness Welcome Kit

Manufacturer
Buzz Export Services Pty., Ltd
Effective date
2022-02-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:42:11

Label at a glance#

ProductMurchison-Hume Wellness Welcome Kit
Active ingredientALCOHOL
Label structure15 sections

Indications and uses

To help reduce bacteria on the skin.

Dosage and administration

Apply to hands or surfaces.  No rinsing required. Discard after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

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.

Flammable

  • Keep away from fire or flame.

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

  • Apply to hands or surfaces.
  •  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 (Tea Tree) Leaf Oil.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

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

  • Squeeze a significant amount in your palm and rub hands until full dry. No rinsing required.

Other Information

SPL UNCLASSIFIED SECTION

  • Store below 110°f (43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Acrylates/C-10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Melaleuca Alternafolia (Tea Tree) Leaf Oil, Aminomethyl Propanol.

Kit Label:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KIT2KIT2

Package Labeling:69491-303-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:69491-301-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69491-305-002024-01-30C16284748780-1d6a99b39-7b84-a426-e053-dadaa90af4c2Murchison-Hume Wellness Welcome Kit
69491-305-002022-12-30C16284748780-1d6a99b39-7b84-a426-e053-dadaa90af4c2Murchison-Hume Wellness Welcome Kit
69491-305-002022-01-28C16284748780-1d6a99b39-7b84-a426-e053-dadaa90af4c2Murchison-Hume Wellness Welcome Kit

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69491-301MURCHISON-HUME WELLNESS WELCOME KIT (ALCOHOL) KIT [BUZZ EXPORT SERVICES PTY., LTD]2Unmatched20230101_697b4ffb-3b1a-4031-8dca-0bbe743565ae.zip
69491-303MURCHISON-HUME WELLNESS WELCOME KIT (ALCOHOL) KIT [BUZZ EXPORT SERVICES PTY., LTD]2Unmatched20230101_697b4ffb-3b1a-4031-8dca-0bbe743565ae.zip
69491-305MURCHISON-HUME WELLNESS WELCOME KIT (ALCOHOL) KIT [BUZZ EXPORT SERVICES PTY., LTD]2Legacy NDC20230101_697b4ffb-3b1a-4031-8dca-0bbe743565ae.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69491-30569491-305-00
69491-30369491-303-00
69491-30169491-301-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
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
0cfd8733-7508-b29f-e063-6394a90ab192697b4ffb-3b1a-4031-8dca-0bbe743565ae2023-12-20WarningsExact identifier
spl set id: 697b4ffb-3b1a-4031-8dca-0bbe743565ae

Reported adverse events (FAERS/openFDA)#

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