NDC 69540-0018 Clorox Oxi Dish Oxi Magic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69540 - Brand Buzz
- 69540-0018 - Clorox Oxi Dish
Product Characteristics
Product Packages
NDC Code 69540-0018-1
Package Description: 768.912 mL in 1 BOTTLE, DISPENSING
Product Details
What is NDC 69540-0018?
What are the uses for Clorox Oxi Dish Oxi Magic?
Which are Clorox Oxi Dish Oxi Magic UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Clorox Oxi Dish Oxi Magic 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- 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".