NDC 20276-906 Personal Care For Men Quick Dry Antiperspirant

Aluminum Chlorohydrate 20.2%

NDC Product Code 20276-906

NDC Code: 20276-906

Proprietary Name: Personal Care For Men Quick Dry Antiperspirant 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 20.2% 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.

Code Structure
  • 20276 - Delta Brands Inc
    • 20276-906 - Personal Care

NDC 20276-906-34

Package Description: 34 g in 1 BOTTLE, SPRAY

NDC 20276-906-45

Package Description: 45 g in 1 BOTTLE, SPRAY

NDC Product Information

Personal Care For Men Quick Dry Antiperspirant with NDC 20276-906 is a a human over the counter drug product labeled by Delta Brands Inc. The generic name of Personal Care For Men Quick Dry Antiperspirant is aluminum chlorohydrate 20.2%. The product's dosage form is spray and is administered via topical form.

Labeler Name: Delta Brands Inc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Personal Care For Men Quick Dry Antiperspirant 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.

  • ALCOHOL (UNII: 3K9958V90M)
  • PROPANE (UNII: T75W9911L6)

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: Delta Brands Inc
Labeler Code: 20276
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: 02-01-2019 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: 12-31-2020 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.

Personal Care For Men Quick Dry Antiperspirant Product Label Images

Personal Care For Men Quick Dry Antiperspirant 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

Aluminum Chlorohydrate 20.2%

Otc - Purpose

Purpose  Antiperspirant

Indications & Usage

Use reduces underarm wetness


Flammable. Do not use near heat, flame or whilesmoking. Can cause serious Injury or death.■ keep away from face and mouth to avoid

breathing in ■ avoid spraying in eyes. Contents

under pressure. Do not puncture or incinerate.

Do not expose to heal or store at temperature

above 120°F/SO"C or in enclosed places that

could overheat ■ do not use on broken skin.

Otc - Stop Use

Stop use if rash or irritation occurs

Otc - Ask Doctor

Ask a doctor before using if you have kidney disease

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Other Safety Information

Use only as directed. Intentional misuse

by deliberately concentrating and Inhaling

the contents can be harmful or fatal.

Help stop inhalation abuse.

For information visit www.inhalant.org

Dosage & Administration

Directions ■ hold can 6 inches away from

the underarm ■ apply to underarms only

Inactive Ingredient

Inactive Ingredientsbutane, hydrofluorocarbon 152A, cyclopentasiloxane, alcohol denat.,

PPG-14 butyl ether, isobutane, propane, disteardimonium, hectorlte, C12-15 alkyl

benzoate, helianthus annuus (sunflower) seed oil, dimethiconol,

propylene carbonate, octyIdodecanol,

fragrance, tocopheryl acetate, BHT

* Please review the disclaimer below.

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