NDC 73306-1112 Antiperspirant Above Soft Creme
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73306 - Baston Industria De Aeross�is Ltda
- 73306-1112 - Antiperspirant Above Soft Creme
Product Characteristics
Product Packages
NDC Code 73306-1112-1
Package Description: 90 g in 1 CAN
Product Details
What is NDC 73306-1112?
Which are Antiperspirant Above Soft Creme UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V)
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (Active Moiety)
Which are Antiperspirant Above Soft Creme 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- LEVANT COTTON SEED (UNII: 550E4N439V)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- COCONUT (UNII: 3RT3536DHY)
- ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
- ALLANTOIN (UNII: 344S277G0Z)
- BUTANE (UNII: 6LV4FOR43R)
- CHAMOMILE (UNII: FGL3685T2X)
- ISOBUTANE (UNII: BXR49TP611)
- MACADAMIA OIL (UNII: 515610SU8C)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SHEA BUTTER (UNII: K49155WL9Y)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- MYRRH OIL (UNII: H74221J5J4)
- PROPANE (UNII: T75W9911L6)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ARGAN OIL (UNII: 4V59G5UW9X)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
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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".