NDC 52083-699 Neogen-d
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52083 - Kramer Novis
- 52083-699 - Neogen-d
Product Characteristics
Product Packages
NDC Code 52083-699-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 52083-699?
What are the uses for Neogen-d?
Which are Neogen-d UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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 Neogen-d 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:
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Neogen-d?
- RxCUI: 1000502 - dextromethorphan HBr 30 MG / guaiFENesin 200 MG / phenylephrine HCl 7.5 MG in 5 mL Oral Solution
- RxCUI: 1000502 - dextromethorphan hydrobromide 6 MG/ML / guaifenesin 40 MG/ML / phenylephrine hydrochloride 1.5 MG/ML Oral Solution
- RxCUI: 1000502 - dextromethorphan HBr 30 MG / guaifenesin 200 MG / phenylephrine HCl 7.5 MG per 5 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".