NDC 53807-503 Kao-bis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53807 - Rij Pharmaceutical Corporation
- 53807-503 - Kao-bis
Product Characteristics
Product Packages
NDC Code 53807-503-08
Package Description: 237 mL in 1 BOTTLE
NDC Code 53807-503-12
Package Description: 355 mL in 1 BOTTLE
NDC Code 53807-503-16
Package Description: 473 mL in 1 BOTTLE
Product Details
What is NDC 53807-503?
What are the uses for Kao-bis?
Which are Kao-bis UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1)
- BISMUTH CATION (UNII: ZS9CD1I8YE) (Active Moiety)
Which are Kao-bis 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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Kao-bis?
- RxCUI: 308762 - bismuth subsalicylate 525 MG in 30 mL Oral Suspension
- RxCUI: 308762 - bismuth subsalicylate 17.5 MG/ML Oral Suspension
- RxCUI: 308762 - bismuth subsalicylate 1.75 % Oral Suspension
- RxCUI: 308762 - bismuth subsalicylate 262 MG per 15 ML Oral Suspension
- RxCUI: 308762 - bismuth subsalicylate 524 MG per 30 ML Oral Suspension
* 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".