NDC 58552-323 Phenagil Ch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58552 - Gil Pharmaceutical Corp
- 58552-323 - Phenagil Ch
Product Characteristics
Product Packages
NDC Code 58552-323-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 58552-323-02
Package Description: 12 POUCH in 1 BOX / 2 TABLET in 1 POUCH
Product Details
What is NDC 58552-323?
What are the uses for Phenagil Ch?
Which are Phenagil Ch UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
- CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y)
- CHLOPHEDIANOL (UNII: 42C50P12AP) (Active Moiety)
Which are Phenagil Ch 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CROSCARMELLOSE (UNII: 029TFK992N)
What is the NDC to RxNorm Crosswalk for Phenagil Ch?
- RxCUI: 1424872 - chlophedianol HCl 24 MG / chlorpheniramine maleate 3.5 MG / phenylephrine HCl 10 MG Oral Tablet
- RxCUI: 1424872 - chlophedianol hydrochloride 24 MG / chlorpheniramine maleate 3.5 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".