NDC 54473-152 Body Satin Antiperspirant And Deodorant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 54473-152?
What are the uses for Body Satin Antiperspirant And Deodorant?
Which are Body Satin Antiperspirant And Deodorant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)
Which are Body Satin Antiperspirant And Deodorant 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- BRAZIL NUT OIL (UNII: 0G89T29HO6)
- BIXA ORELLANA SEED (UNII: O87354RZ5A)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PEG-8 DISTEARATE (UNII: 7JNC8VN07M)
- PPG-14 BUTYL ETHER (UNII: R199TJT95T)
- PLANTAGO LANCEOLATA LEAF (UNII: 2YWL9J7EE8)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TALC (UNII: 7SEV7J4R1U)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- STARCH, CORN (UNII: O8232NY3SJ)
* Please review the disclaimer below.
[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".