NDC 65923-626 Family Care Stomach Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65923 - United Exchange Corp.
- 65923-626 - Family Care Stomach Relief
Product Packages
NDC Code 65923-626-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 65923-626?
What are the uses for Family Care Stomach Relief?
Which are Family Care Stomach Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Family Care Stomach Relief 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:
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MENTHOL (UNII: L7T10EIP3A)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SORBIC ACID (UNII: X045WJ989B)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Family Care Stomach Relief?
- RxCUI: 308763 - bismuth subsalicylate 1050 MG in 30 mL Oral Suspension
- RxCUI: 308763 - bismuth subsalicylate 35 MG/ML Oral Suspension
- RxCUI: 308763 - bismuth subsalicylate 1050 MG per 30 ML Oral Suspension
- RxCUI: 308763 - bismuth subsalicylate 525 MG per 15 ML Oral Suspension
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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".