NDC 43596-0201 Pulso Absolute Antiperspirant Roll-on Deodorant
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation Limited
- 43596-0201 - Pulso Absolute Antiperspirant Roll-on Deodorant
Product Packages
NDC Code 43596-0201-1
Package Description: 50 mL in 1 JAR
Product Details
What is NDC 43596-0201?
What are the uses for Pulso Absolute Antiperspirant Roll-on Deodorant?
Which are Pulso Absolute Antiperspirant Roll-on Deodorant 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 Pulso Absolute Antiperspirant Roll-on 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:
- GERANIOL (UNII: L837108USY)
- CITRAL (UNII: T7EU0O9VPP)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- STEARETH-21 (UNII: 53J3F32P58)
- STEARETH-2 (UNII: V56DFE46J5)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- EDETATE SODIUM (UNII: MP1J8420LU)
- LEVOMENOL (UNII: 24WE03BX2T)
- COUMARIN (UNII: A4VZ22K1WT)
- PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- WATER (UNII: 059QF0KO0R)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
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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".