NDC 53247-116 Bob Barker Antibacterial Unwrapped Body
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53247 - Bob Barker Company Inc.
- 53247-116 - Bob Barker Antibacterial Unwrapped Body
Product Packages
NDC Code 53247-116-01
Package Description: 1000 APPLICATOR in 1 CASE / 11 g in 1 APPLICATOR
NDC Code 53247-116-02
Package Description: 500 APPLICATOR in 1 CASE / 32 g in 1 APPLICATOR
NDC Code 53247-116-03
Package Description: 144 APPLICATOR in 1 CASE / 75 g in 1 APPLICATOR
NDC Code 53247-116-04
Package Description: 200 APPLICATOR in 1 CASE / 85 g in 1 APPLICATOR
Product Details
What is NDC 53247-116?
What are the uses for Bob Barker Antibacterial Unwrapped Body?
Which are Bob Barker Antibacterial Unwrapped Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
- CHLOROXYLENOL (UNII: 0F32U78V2Q) (Active Moiety)
Which are Bob Barker Antibacterial Unwrapped Body 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:
- SODIUM PALMATE (UNII: S0A6004K3Z)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- WATER (UNII: 059QF0KO0R)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- PALM OIL (UNII: 5QUO05548Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ETIDRONIC ACID (UNII: M2F465ROXU)
What is the NDC to RxNorm Crosswalk for Bob Barker Antibacterial Unwrapped Body?
- RxCUI: 2172091 - chloroxylenol 0.1 % MG/MG Medicated Bar Soap
- RxCUI: 2172091 - chloroxylenol 0.001 MG/MG Medicated Bar 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".