NDC 64942-1322 Degree Adrenaline Adventure Antiperspirant And Deodorant
NDC Product 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
- 64942 - Conopco Inc. D/b/a Unilever
- 64942-1322 - Degree
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)
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
- Otc - Purpose
- Indications & Usage
- Warnings
- Otc - Do Not Use
- Otc - Ask Doctor
- Otc - Stop Use
- Otc - Keep Out Of Reach Of Children
- Dosage & Administration
- Inactive Ingredient
- Otc - Questions
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.