NDC 68210-1901 Simethicone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68210 - Spirit Pharmaceuticals,llc
- 68210-1901 - Simethicone
Product Characteristics
Product Packages
NDC Code 68210-1901-1
Package Description: 10 CAPSULE, LIQUID FILLED in 1 BOX
NDC Code 68210-1901-2
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOX
NDC Code 68210-1901-3
Package Description: 1000 CAPSULE, LIQUID FILLED in 1 BOX
NDC Code 68210-1901-4
Package Description: 16000 CAPSULE, LIQUID FILLED in 1 BOX
NDC Code 68210-1901-5
Package Description: 20000 CAPSULE, LIQUID FILLED in 1 BOX
Product Details
What is NDC 68210-1901?
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)
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:
- GLYCERIN (UNII: PDC6A3C0OX)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Simethicone?
- RxCUI: 198852 - simethicone 125 MG Oral Capsule
- RxCUI: 198852 - dimethicone 125 MG Oral Capsule
* 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".