NDC 50090-4856 Guaifenesin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
VANILLA (C73421 - ARTIFICIAL VANILLA FLAVOR)
Code Structure Chart
Product Details
What is NDC 50090-4856?
What are the uses for Guaifenesin?
Which are Guaifenesin UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Guaifenesin 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- ASPARTAME (UNII: Z0H242BBR1)
- HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Guaifenesin?
- RxCUI: 310604 - guaiFENesin 100 MG in 5 mL Oral Solution
- RxCUI: 310604 - guaifenesin 20 MG/ML Oral Solution
- RxCUI: 310604 - guaifenesin 100 MG per 5 ML Oral Solution
- RxCUI: 310604 - guaifenesin 100 MG per 5 ML Oral Syrup
- RxCUI: 310604 - guaifenesin 200 MG per 10 ML Oral Solution
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Patient Education
Guaifenesin
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
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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".