NDC 69491-305 Murchison-hume Wellness Welcome Kit

Alcohol

NDC Product Code 69491-305

NDC 69491-305-00

Package Description: 1 KIT in 1 KIT * 1 PATCH in 1 PACKAGE (69491-303-00) > 5 mL in 1 PATCH * 20 mL in 1 BOTTLE (69491-301-00)

NDC Product Information

Murchison-hume Wellness Welcome Kit with NDC 69491-305 is a a human over the counter drug product labeled by Buzz Products (hk) Co. Limited. The generic name of Murchison-hume Wellness Welcome Kit is alcohol. The product's dosage form is kit and is administered via form.

Labeler Name: Buzz Products (hk) Co. Limited

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
  • 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)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Buzz Products (hk) Co. Limited
Labeler Code: 69491
FDA Application Number: part333E What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-30-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Murchison-hume Wellness Welcome Kit Product Label Images

Murchison-hume Wellness Welcome Kit Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Ethyl Alcohol 75% (v/v)

Ethyl Alcohol 75% (v/v)

Purpose

Antiseptic

Antiseptic

Uses

  • To help reduce bacteria on the skin.

To help reduce bacteria on the skin.

Warnings

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

  • 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.

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

Stop Using And Ask A Doctor If

  • Irritation or redness develops and lasts.

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.

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.

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

Other Information

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

  • Store below 110°f (43°C).

Inactive Ingredients

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

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

* Please review the disclaimer below.