NDC 30142-773 Kroger Allergy Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 30142-773?
What are the uses for Kroger Allergy Relief?
Which are Kroger Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRILAMINE MALEATE (UNII: R35D29L3ZA)
- PYRILAMINE (UNII: HPE317O9TL) (Active Moiety)
- CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y)
- CHLOPHEDIANOL (UNII: 42C50P12AP) (Active Moiety)
Which are Kroger Allergy Relief 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Kroger Allergy Relief?
- RxCUI: 2672917 - chlophedianol HCl 25 MG / pyrilamine maleate 50 MG in 30 mL Oral Solution
- RxCUI: 2672917 - chlophedianol hydrochloride 0.833 MG/ML / pyrilamine maleate 1.67 MG/ML Oral Solution
- RxCUI: 2672917 - chlophedianol hydrochloride 12.5 MG / pyrilamine maleate 25 MG per 15 ML Oral Solution
- RxCUI: 2672917 - chlophedianol hydrochloride 25 MG / pyrilamine maleate 50 MG per 30 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".