NDC 76413-335 Diabetic Tussin Expectorant

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:
76413-335
Proprietary Name:
Diabetic Tussin Expectorant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Central Texas Community Health Centers
Labeler Code:
76413
Start Marketing Date: [9]
01-01-1996
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - ARTIFICIAL CHERRY FLAVOR)
VANILLA (C73421 - ARTIFICIAL VANILLA FLAVOR)

Product Packages

NDC Code 76413-335-01

Package Description: 118 mL in 1 BOTTLE

Product Details

What is NDC 76413-335?

The NDC code 76413-335 is assigned by the FDA to the product Diabetic Tussin Expectorant which is product labeled by Central Texas Community Health Centers. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76413-335-01 118 ml in 1 bottle . 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 Diabetic Tussin Expectorant?

Take every 4 hoursdo not exceed 6 doses in 24 hoursadults & children 12 years and over 10 mL - 20 mL (2 - 4 teaspoonfuls)children 6 years to under 12 years5 mL - 10 mL (1 - 2 teaspoonfuls)children 2 years to under 6 years2.5 mL - 5 mL (½ - 1 teaspoonful)children under 2 years ask a doctor

Which are Diabetic Tussin Expectorant UNII Codes?

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

Which are Diabetic Tussin Expectorant 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 Diabetic Tussin Expectorant?

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:

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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".