NDC 30142-771 Kroger Cough Cold And Flu
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 30142 - The Kroger Co
- 30142-771 - Kroger Cough Cold And Flu
Product Packages
NDC Code 30142-771-08
Package Description: 237 mL in 1 BOTTLE
Product Details
What is NDC 30142-771?
What are the uses for Kroger Cough Cold And Flu?
Which are Kroger Cough Cold And Flu UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHOLINE SALICYLATE (UNII: KD510K1IQW)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Kroger Cough Cold And Flu 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:
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Kroger Cough Cold And Flu?
- RxCUI: 1653134 - choline salicylate 870 MG / dextromethorphan HBr 20 MG / guaiFENesin 200 MG / phenylephrine HCl 10 MG in 30 mL Oral Solution
- RxCUI: 1653134 - choline salicylate 29 MG/ML / dextromethorphan hydrobromide 0.67 MG/ML / guaifenesin 6.67 MG/ML / phenylephrine hydrochloride 0.33 MG/ML Oral Solution
- RxCUI: 1653134 - choline salicylate 870 MG / dextromethorphan HBr 20 MG / guaifenesin 200 MG / phenylephrine HCl 10 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".