NDC 64092-208 Antiperspirant Invisible Powder Fresh

Aluminum Chlorohydrate

NDC Product Code 64092-208

NDC CODE: 64092-208

Proprietary Name: Antiperspirant Invisible Powder Fresh 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.

Product Characteristics

WHITE (C48325)

NDC Code Structure

  • 64092 - Great Lakes Wholesale, Marketing And Sales, Inc

NDC 64092-208-02

Package Description: 57 g in 1 DIALPACK

NDC Product Information

Antiperspirant Invisible Powder Fresh with NDC 64092-208 is a a human over the counter drug product labeled by Great Lakes Wholesale, Marketing And Sales, Inc. The generic name of Antiperspirant Invisible Powder Fresh 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.

Antiperspirant Invisible Powder Fresh 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: Great Lakes Wholesale, Marketing And Sales, Inc
Labeler Code: 64092
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: 06-30-2016 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.

Antiperspirant Invisible Powder Fresh Product Label Images

Antiperspirant Invisible Powder Fresh 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


GLS PERSONAL CARE SOLUTIONSSolid InvisiblePowder FreshAntiperspirant DeodorantNet WT. 2 OZ (57 g)

Otc - Active Ingredient

Active Ingredients PurposeAluminum chlorohydrates 20%............................Antiperspirant

Otc - Purpose

Reduce underarm wetness and perspiration


For external use onlyDo not use on broken or irritated skinStop use an ask a doctor if irritation or rash develops

Otc - Keep Out Of Reach Of Children

If swallowed, seek medical help or contact a poison control center immediately.

Instructions For Use

Remove cap, turn dial to raise product, apply evenly to underarms only. replace cap after use.

Dosage & Administration

Stick antipirspirant deodorant20% aluminum chlorohydrates

Indications & Usage

To reduce underarm wetness and perspiration

Inactive Ingredient

Mineral oil, stearic acid, stearyl alcohol, talc, zinc palmitate, cyclopentasiloxane, hydrogenated castor oil, fragrance, silica, PPG-14, butyl ether, PEG-8 distearate, BHT.

* Please review the disclaimer below.