NDC 64942-1445 Degree Motionsense Ultraclear Black And White Pure Clean Dry Antiperspirant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco Inc. D/b/a/ Unilever
- 64942-1445 - Degree
Product Packages
NDC Code 64942-1445-1
Package Description: 107 g in 1 CAN
Product Details
What is NDC 64942-1445?
What are the uses for Degree Motionsense Ultraclear Black And White Pure Clean Dry Antiperspirant?
Which are Degree Motionsense Ultraclear Black And White Pure Clean Dry Antiperspirant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)
Which are Degree Motionsense Ultraclear Black And White Pure Clean Dry Antiperspirant Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- BUTANE (UNII: 6LV4FOR43R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
- ISOBUTANE (UNII: BXR49TP611)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PROPANE (UNII: T75W9911L6)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".