NDC 13537-505 Esika Total Sec Delicate Skin Alcohol Free Womens Deodorant And Antiperspirant - All Day Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd.
- 13537-505 - Esika
Product Packages
NDC Code 13537-505-01
Package Description: 125 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 13537-505?
What are the uses for Esika Total Sec Delicate Skin Alcohol Free Womens Deodorant And Antiperspirant - All Day Protection?
Which are Esika Total Sec Delicate Skin Alcohol Free Womens Deodorant And Antiperspirant - All Day Protection 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 Esika Total Sec Delicate Skin Alcohol Free Womens Deodorant And Antiperspirant - All Day Protection 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)
- ISOBUTANE (UNII: BXR49TP611)
- PROPANE (UNII: T75W9911L6)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- LEVOMENOL (UNII: 24WE03BX2T)
- TRICLOSAN (UNII: 4NM5039Y5X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- BAMBUSA BAMBOS LEAF (UNII: HW86D1FGSS)
* 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".