NDC 64942-1511 Axe
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco Inc. D/b/a/ Unilever
- 64942-1511 - Axe
Product Packages
NDC Code 64942-1511-1
Package Description: 107 g in 1 CAN
Product Details
What is NDC 64942-1511?
What are the uses for Axe?
Which are Axe 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 Axe 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)
- 1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISOBUTANE (UNII: BXR49TP611)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- PROPANE (UNII: T75W9911L6)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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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".