NDC 64942-1373 Axe Night Antiperspirant

Aluminum Chlorohydrate

NDC Product Code 64942-1373

NDC 64942-1373-1

Package Description: 107 g in 1 CAN

NDC 64942-1373-2

Package Description: 28 g in 1 CAN

NDC Product Information

Axe Night Antiperspirant with NDC 64942-1373 is a a human over the counter drug product labeled by Conopco Inc. D/b/a Unilever. The generic name of Axe Night Antiperspirant is aluminum chlorohydrate. The product's dosage form is aerosol, spray and is administered via topical form.

Dosage Form: Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.

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.

Axe Night 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.

  • BUTANE (UNII: 6LV4FOR43R)
  • 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • ISOBUTANE (UNII: BXR49TP611)
  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • PROPANE (UNII: T75W9911L6)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)

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: Conopco Inc. D/b/a Unilever
Labeler Code: 64942
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: 11-01-2014 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.

Axe Night Antiperspirant Product Label Images

Axe Night 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

Otc - Active Ingredient

Active ingredientAluminum chlorohydrate (23.3%)

Otc - Purpose

Purposeanti-perspirant

Indications & Usage

Uses· reduces underarm wetness

Warnings

WARNINGSFor external use only• FLAMMABLE.  DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING.  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 heat or store at temperatures above 120 degrees F/50 degrees C or in enclosed places that could overheat.• Do not use on broken skin. Stop use if rash or irritation occurs.• Ask a doctor before using if you have kidney disease.• 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

Otc - Keep Out Of Reach Of Children

• KEEP OUT OF REACH OF CHILDREN

Dosage & Administration

Directions  Apply to underarms only.  If dispenser clogs, rinse in warm water.

Inactive Ingredient

Inactive ingredientsButane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propane, BHT, Propylene Carbonate

Otc - Questions

Questions?Call toll-free 1-800-450-7580

* Please review the disclaimer below.