NDC 43378-124 Zodryl Dec 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43378 - Codadose, Inc.
- 43378-124 - Zodryl Dec 50
Product Characteristics
Product Packages
NDC Code 43378-124-08
Package Description: 236 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43378-124?
What are the uses for Zodryl Dec 50?
Which are Zodryl Dec 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
- CODEINE PHOSPHATE (UNII: GSL05Y1MN6)
- CODEINE (UNII: Q830PW7520) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Zodryl Dec 50 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- TANNIC ACID (UNII: 28F9E0DJY6)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Zodryl Dec 50?
- RxCUI: 1089028 - codeine phosphate 1 MG/ML / guaifenesin 20 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Suspension
- RxCUI: 1089028 - codeine phosphate 1 MG / guaifenesin 20 MG / pseudoephedrine hydrochloride 6 MG per 1 ML Oral Suspension
- RxCUI: 1089030 - codeine phosphate 1 MG/ML / guaifenesin 20 MG/ML / pseudoephedrine hydrochloride 6 MG/ML Oral Suspension [Zodryl DEC]
- RxCUI: 1089030 - Zodryl DEC 50 (codeine phosphate 1 MG / guaifenesin 20 MG / pseudoephedrine hydrochloride 6 MG) per 1 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".