NDC 52083-699 Neogen-d

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52083-699
Proprietary Name:
Neogen-d
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kramer Novis
Labeler Code:
52083
Start Marketing Date: [9]
10-10-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
RASPBERRY (C73413)

Product Packages

NDC Code 52083-699-16

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 52083-699?

The NDC code 52083-699 is assigned by the FDA to the product Neogen-d which is product labeled by Kramer Novis. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52083-699-16 473 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Neogen-d?

Do not take more than 4 doses in any 24-hour period. Shake well before using.Every 6-8 hours Adults and children 12 years of age and over Take one teaspoonful (5 mL) Children 6 to under 12 years of age  Take 1/2 teaspoonful (2.5 mL) Children under 6 years of age Consult a doctor

Which are Neogen-d UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Neogen-d?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[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".