NDC 11856-0026 Goyescas 7 Syrups With Bee Honey Cough And Cold
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11856 - Goyescas Of Fla
- 11856-0026 - Goyescas 7 Syrups With Bee Honey
Product Packages
NDC Code 11856-0026-1
Package Description: 1 BOTTLE in 1 BOX / 177 mL in 1 BOTTLE
Product Details
What is NDC 11856-0026?
What are the uses for Goyescas 7 Syrups With Bee Honey Cough And Cold?
Which are Goyescas 7 Syrups With Bee Honey Cough And Cold UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
Which are Goyescas 7 Syrups With Bee Honey Cough And Cold 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:
- GINGER (UNII: C5529G5JPQ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- HONEY (UNII: Y9H1V576FH)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Goyescas 7 Syrups With Bee Honey Cough And Cold?
- RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 10 mL Oral Solution
- RxCUI: 1044949 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 1 MG/ML Oral Solution
- RxCUI: 1044949 - dextromethorphan HBr 10 MG / guaifenesin 100 MG / phenylephrine HCl 5 MG per 5 ML Oral Solution
- RxCUI: 1044949 - dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 MG per 10 ML Oral Solution
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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".