NDC 54868-5620 Simethicone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5620 - Simethicone
Product Packages
NDC Code 54868-5620-0
Package Description: 1 BOTTLE in 1 CARTON / 30 mL in 1 BOTTLE
Product Details
What is NDC 54868-5620?
What are the uses for Simethicone?
Which are Simethicone UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are Simethicone 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:
- CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
What is the NDC to RxNorm Crosswalk for Simethicone?
- RxCUI: 198857 - simethicone 20 MG in 0.3 mL Oral Suspension
- RxCUI: 198857 - simethicone 66.7 MG/ML Oral Suspension
- RxCUI: 198857 - simethicone 20 MG per 0.3 ML Oral Suspension
- RxCUI: 198857 - simethicone 40 MG per 0.6 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".