NDC 0031-8724 Robitussin Mucus Plus Chest Congestion
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0031 - Richmond Division Of Wyeth
- 0031-8724 - Robitussin Mucus Plus Chest Congestion
Product Characteristics
Product Packages
NDC Code 0031-8724-12
Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Price per Unit: $0.05997 per ML
Product Details
What is NDC 0031-8724?
What are the uses for Robitussin Mucus Plus Chest Congestion?
Which are Robitussin Mucus Plus Chest Congestion UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Robitussin Mucus Plus Chest Congestion 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)
- CARAMEL (UNII: T9D99G2B1R)
- DEXTROSE (UNII: IY9XDZ35W2)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- PROPYLENE GLYCOL, (R)- (UNII: 602HN5L69H)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Robitussin Mucus Plus Chest Congestion?
- 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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[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".