NDC 50481-3300 Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice

Aluminum Chlorohydrate

NDC Product Code 50481-3300

NDC CODE: 50481-3300

Proprietary Name: Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aluminum Chlorohydrate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 50481 - Kcm Brands Llc
    • 50481-3300 - Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice

NDC 50481-3300-1

Package Description: 48 g in 1 CONTAINER

NDC Product Information

Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice with NDC 50481-3300 is a a human over the counter drug product labeled by Kcm Brands Llc. The generic name of Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice is aluminum chlorohydrate. The product's dosage form is stick and is administered via topical form.

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

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.

Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice 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.


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: Kcm Brands Llc
Labeler Code: 50481
FDA Application Number: part350 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 01-27-2010 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.

Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice Product Label Images

Tussy Antiperspirant And Deodorant Invisible Original Fresh Spice 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

Otc - Active Ingredient

Active Ingredients                                            PurposeAluminum Chlorohydrate 20 percent            Antiperspirant

Otc - Purpose

Use reduces underarm perspiration


WarningsFor external use only

Otc - Ask Doctor

Ask a doctor before use- if you have kidney disease

Otc - When Using

When using this product -  do not use on broken skinStop use if rash or irritation occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Dosage & Administration

DirectionsApply evenly to underarms onlyUse daily as needed

Indications & Usage

Other InformationTo ensure product appears clear on skin, do not over-apply

Inactive Ingredient

Inactive IngredientsStearyl Alcohol,  Cetyl Alcohol, Hydrogenated Castor Oil, talc, Glyceryl Stearate, PEG 100 Stearate, Fragrance, BHT


Distributed By:KCM Brands, Inc.2182 Route 35 SouthHolmdel, NJ 07733

* Please review the disclaimer below.