NDC 0363-0601 Walgreens Wal-flu Cold And Sore Throat Lemon Flavor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
RED (C48326 - FD AND C RED 40)
Code Structure Chart
Product Details
What is NDC 0363-0601?
What are the uses for Walgreens Wal-flu Cold And Sore Throat Lemon Flavor?
Which are Walgreens Wal-flu Cold And Sore Throat Lemon Flavor UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- PHENIRAMINE MALEATE (UNII: NYW905655B)
- PHENIRAMINE (UNII: 134FM9ZZ6M) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Walgreens Wal-flu Cold And Sore Throat Lemon Flavor 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ETHYLCELLULOSE (100 MPA.S) (UNII: 47MLB0F1MV)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCROSE (UNII: C151H8M554)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
What is the NDC to RxNorm Crosswalk for Walgreens Wal-flu Cold And Sore Throat Lemon Flavor?
- RxCUI: 1796460 - acetaminophen 325 MG / pheniramine maleate 20 MG / phenylephrine HCl 10 MG Powder for Oral Solution
- RxCUI: 1796460 - acetaminophen 325 MG / pheniramine maleate 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
- RxCUI: 1796460 - acetaminophen 325 MG / pheniramine maleate 20 MG / phenylephrine hydrochloride 10 MG Granule for Oral Solution
- RxCUI: 1796460 - acetaminophen 325 MG / pheniramine maleate 20 MG / phenylephrine hydrochloride 10 MG Packet for Oral Solution
- RxCUI: 1796460 - APAP 325 MG / Pheniramine Maleate 20 MG / Phenylephrine Hydrochloride 10 MG Powder for 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".