NDC 63691-031 Publix Green Apple Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63691 - Sun Products Corporation
- 63691-031 - Publix Green Apple Scent
Product Characteristics
Product Packages
NDC Code 63691-031-10
Package Description: 709 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 63691-031?
What are the uses for Publix Green Apple Scent?
Which are Publix Green Apple Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Publix Green Apple Scent 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:
- EDETATE SODIUM (UNII: MP1J8420LU)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
What is the NDC to RxNorm Crosswalk for Publix Green Apple Scent?
- RxCUI: 413261 - chloroxylenol 0.3 % Medicated Liquid Soap
- RxCUI: 413261 - chloroxylenol 3 MG/ML Medicated Liquid Soap
* 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".