Murchison-Hume Wellness Welcome Kit

Murchison-Hume Wellness Welcome Kit by

Drug Labeling and Warnings

Murchison-Hume Wellness Welcome Kit by is a Otc medication manufactured, distributed, or labeled by Buzz Export Services Pty., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MURCHISON-HUME WELLNESS WELCOME KIT- alcohol 
Buzz Products Inc

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Murchison-Hume Wellness Welcome Kit

Drug Facts

Active Ingredient

Ethyl Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

  • To help reduce bacteria on the skin.

Warnings

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

Flammable

When using this product

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

Stop using and ask a doctor if

  • irritation or redness develops and lasts.

Keep out of reach of children

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

Directions

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

Other Information

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

Inactive ingredients

Aqua (Water), Glycerin. Polyquaternium-37, Melaleuca Alternifolia (Tea Tree) Leaf Oil.

Drug Facts

Active Ingredient

Ethyl Alcohol 75% (v/v)

Purpose

Antiseptic

Uses

To help reduce bacteria on the skin.

Warnings

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

When using this product

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

Stop using and ask a doctor if

irritation or redness develops and lasts.

Keep out of reach of children

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

Directions

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

Other Information

  • Store below 110°f (43°C).

Inactive ingredients

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

Kit Label:

KIT2

Package Labeling:69491-303-00

Label2

Package Labeling:69491-301-00

Label.

MURCHISON-HUME WELLNESS WELCOME KIT 
alcohol kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69491-305
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69491-305-001 in 1 KIT09/30/202011/30/2025
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 PATCH 5 mL
Part 21 BOTTLE 20 mL
Part 1 of 2
MURCHISON-HUME SANITIZING WIPE WITH TEA TREE OIL 75% ALCOHOL 
alcohol cloth
Product Information
Item Code (Source)NDC: 69491-303
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69491-303-001 in 1 PACKAGE
15 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/30/202011/30/2025
Part 2 of 2
HAND SANITIZER WITH TEA TREE OIL 75% ALCOHOL 
alcohol gel
Product Information
Item Code (Source)NDC: 69491-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69491-301-0020 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/30/202011/30/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/30/202011/30/2025
Labeler - Buzz Products Inc (144902952)

Revised: 12/2023
 

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