NDC 64942-1322 Degree Adrenaline Adventure Antiperspirant And Deodorant

  1. Labeler Index
  2. Conopco Inc. D/b/a Unilever
  3. NDC: 64942-1322 Degree Adrenaline Adventure Antiperspirant And Deodorant

NDC Product Code 64942-1322

NDC CODE: 64942-1322

Proprietary Name: Degree Adrenaline Adventure Antiperspirant And Deodorant 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: 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

NDC 64942-1322-2

Package Description: 48 g in 1 CONTAINER

NDC 64942-1322-3

Package Description: 14 g in 1 CONTAINER

NDC 64942-1322-5

Package Description: 2 PACKAGE in 1 PACKAGE > 2 CONTAINER in 1 PACKAGE (64942-1322-4) > 76 g in 1 CONTAINER (64942-1322-1)

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Degree Adrenaline Adventure Antiperspirant And Deodorant with NDC 64942-1322 is a product labeled by Conopco Inc. D/b/a Unilever. The generic name of Degree Adrenaline Adventure Antiperspirant And Deodorant is . The product's dosage form is and is administered via form.

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

Dosage Form: -

Product Type: 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.

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.
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • PPG-14 BUTYL ETHER (UNII: R199TJT95T)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
  • TALC (UNII: 7SEV7J4R1U)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • HYDRATED SILICA (UNII: Y6O7T4G8P9)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)

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
Start Marketing Date: 12-02-2013 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: 12-31-2019 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: I 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 Adrenaline Adventure Antiperspirant And Deodorant Product Label Images

Degree Adrenaline Adventure Antiperspirant And Deodorant 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 Zirconium Tetrachlorohydrex GLY (19.2%)

Otc - Purpose

Purposeantiperspirant

Indications & Usage

Usesreduces underarm wetness

Warnings

WarningsFor external use only

Otc - Do Not Use

Do not use on broken skin

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease

Otc - Stop Use

Stop 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 to underarms only

Inactive Ingredient

Inactive ingredients: Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Fragrance (Parfum), Talc, PEG-8 Distearate, Caprylic/Capric Triglyceride, Sodium Starch Octenylsuccinate, Hydrated Silica, Maltodextrin, Gelatin Crosspolymer, Hydrolyzed Corn Starch, BHT, Silica, Cellulose Gum

Otc - Questions

Questions?Call toll-free 1-866-334-7331

* Please review the disclaimer below.