NDC 50241-333 Sono Healthcare


NDC Product Code 50241-333

NDC 50241-333-00

Package Description: 480 g in 1 BOTTLE, PLASTIC

NDC Product Information

Sono Healthcare with NDC 50241-333 is a a human over the counter drug product labeled by Morgan Gallacher Inc.. The generic name of Sono Healthcare is n/a. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Morgan Gallacher Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Sono Healthcare Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Morgan Gallacher Inc.
Labeler Code: 50241
FDA Application Number: part333A 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: 03-18-2020 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Sono Healthcare Product Label Images

Sono Healthcare 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

Benzalkonium Chloride.........0.13 %


Antiseptic hand sanitizer


  • Hand sanitizer to help reduce bacteria on skinRecommended for repeated use


  • For external use only.Do not use in ears or mouth

When Using This Product

  • Avoid contact with eyes.  In case of contact, flush eyes with water.

Stop Use And Ask A Doctor

  • If redness or irritation develops and persists for more than 72 hours.

Keep Out Of Reach Of Children

Children should be supervised when using this product.


  • Apply a small amount onto hand then spread on both hands. Rub hands together until dry.

Inert Ingredients

  • GlycerinPEG/PPG-18/18 DimethiconeWaterCitrus Aurantium Bergamia Fruit Oil

Sono Healthcare Foaming Hand Sanitizer

* With moisturizer and Bergamot essential oil* Kills 99.99% of most common germs 480mL

* Please review the disclaimer below.