NDC 36800-777 Topcare Cough Cold And Flu Simple Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 36800-777?
What are the uses for Topcare Cough Cold And Flu Simple Relief?
Which are Topcare Cough Cold And Flu Simple Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHOLINE SALICYLATE (UNII: KD510K1IQW)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Topcare Cough Cold And Flu Simple 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Topcare Cough Cold And Flu Simple Relief?
- 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
* Please review the disclaimer below.
[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".