NDC 63868-752 Quality Choice Mucus Relief Pe PE
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63868 - Chain Drug Marketing Association
- 63868-752 - Quality Choice Mucus Relief Pe
Product Characteristics
Product Packages
NDC Code 63868-752-50
Package Description: 1 BOTTLE in 1 CARTON / 50 TABLET in 1 BOTTLE
Product Details
What is NDC 63868-752?
What are the uses for Quality Choice Mucus Relief Pe PE?
Which are Quality Choice Mucus Relief Pe PE 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)
Which are Quality Choice Mucus Relief Pe PE 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE (UNII: J2B2A4N98G)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MINERAL OIL (UNII: T5L8T28FGP)
- POVIDONE (UNII: FZ989GH94E)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Quality Choice Mucus Relief Pe PE?
- RxCUI: 1304111 - guaiFENesin 400 MG / phenylephrine HCl 10 MG Oral Tablet
- RxCUI: 1304111 - guaifenesin 400 MG / phenylephrine hydrochloride 10 MG Oral Tablet
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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".