NDC 37205-295 Leader Gas Relief Extra Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37205 - Cardinal Health
- 37205-295 - Leader Gas Relief
Product Characteristics
Product Packages
NDC Code 37205-295-65
Package Description: 3 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Price per Unit: $0.06476 per EA
Product Details
What is NDC 37205-295?
What are the uses for Leader Gas Relief Extra Strength?
Which are Leader Gas Relief Extra Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Leader Gas Relief Extra Strength 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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- WATER (UNII: 059QF0KO0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Leader Gas Relief Extra Strength?
- RxCUI: 198852 - simethicone 125 MG Oral Capsule
- RxCUI: 198852 - dimethicone 125 MG Oral Capsule
* Please review the disclaimer below.
Patient Education
Simethicone
Simethicone is used to treat the symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* 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".