NDC 50942-008 Antiperspirant Dry 2 Oz Men
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50942 - Zhejiang Ludao Cosmetics Co., Ltd.
- 50942-008 - Antiperspirant Dry 2 Oz Men
Product Packages
NDC Code 50942-008-01
Package Description: 56.7 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 50942-008?
What are the uses for Antiperspirant Dry 2 Oz Men?
Which are Antiperspirant Dry 2 Oz Men 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 Antiperspirant Dry 2 Oz Men 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ISOBUTANE (UNII: BXR49TP611)
- 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- PROPANE (UNII: T75W9911L6)
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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".