NDC 81892-116 Farewell Collection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81892 - Paveemol Company Limited
- 81892-116 - Farewell Collection
Product Packages
NDC Code 81892-116-11
Package Description: 250 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 81892-116?
What are the uses for Farewell Collection?
Which are Farewell Collection UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Farewell Collection 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:
- CHLORPHENESIN (UNII: I670DAL4SZ)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PANTHENOL (UNII: WV9CM0O67Z)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".