NDC 49738-731 Image Essentials Gold
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49738 - Kmart Corporation
- 49738-731 - Image Essentials Gold
Product Packages
NDC Code 49738-731-12
Package Description: 1 CELLO PACK in 1 CARTON / 113 g in 1 CELLO PACK
Product Details
What is NDC 49738-731?
What are the uses for Image Essentials Gold?
Which are Image Essentials Gold UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRICLOCARBAN (UNII: BGG1Y1ED0Y)
- TRICLOCARBAN (UNII: BGG1Y1ED0Y) (Active Moiety)
Which are Image Essentials Gold 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 TALLOWATE, BEEF (UNII: 07RIK6QMEW)
- SODIUM COCOATE (UNII: R1TQH25F4I)
- SODIUM PALMATE (UNII: S0A6004K3Z)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PALM ACID (UNII: B6G0Y5Z616)
- PEG-6 METHYL ETHER (UNII: WXH089JZ5E)
- SORBITOL (UNII: 506T60A25R)
- ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
- PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Image Essentials Gold?
- RxCUI: 1426615 - triclocarban 0.3 % Medicated Bar Soap
- RxCUI: 1426615 - triclocarban 0.003 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".