NDC 64942-1657 Degree

Aluminum Chlorohydrate

NDC Product Code 64942-1657

NDC Product Information

Degree with NDC 64942-1657 is a a human over the counter drug product labeled by Conopco, Inc. D/b/a Unilever. The generic name of Degree is aluminum chlorohydrate. The product's dosage form is aerosol, spray and is administered via topical form.

Labeler Name: Conopco, Inc. D/b/a Unilever

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.

Degree 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.

  • ALUMINUM CHLOROHYDRATE 20.2 g/100g

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.

  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)
  • BUTANE (UNII: 6LV4FOR43R)
  • 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • ISOBUTANE (UNII: BXR49TP611)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • PROPANE (UNII: T75W9911L6)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)
  • DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

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: 08-01-2019 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.

Degree 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

Degree All Day Protection To Move More Dry Spray Now United Antiperspirant Deodoran - Aluminum Chlorohydrate Aerosol, Spray

Degree All Day Protection to Move More Dry Spray Now United Antiperspirant Deodorant

Drug Facts

Active ingredientAluminum Chlorohydrate (20.2%)

Purpose

Antiperspirant

Uses

Reduces underarm wetness

Warnings

• 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°F/50°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

Directions

Apply to underarms only

Inactive Ingredients

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Disteardimonium Hectorite, C12-15 Alkyl Benzoate, Propane, BHT, Octyldodecanol, Propylene Carbonate, Dimethiconol, Tocopheryl Acetate.

Questions?

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