NDC 14505-488 Bisolvine Child

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:
14505-488
Proprietary Name:
Bisolvine Child
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmalab Enterprises Inc.
Labeler Code:
14505
Start Marketing Date: [9]
02-18-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
STRAWBERRY (C73417 - STRAWBERRY -BANANA FLAVOR)

Product Packages

NDC Code 14505-488-04

Package Description: 120 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 14505-488?

The NDC code 14505-488 is assigned by the FDA to the product Bisolvine Child which is product labeled by Pharmalab Enterprises Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 14505-488-04 120 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 Bisolvine Child?

Directions   Do not exceed 6 doses in 24 hours Age                                                                    DoseChildren 6 to under                               1 tablespoonful (15 mL)12 years of age                                    every 4 hoursChildren 2 to under                               1/2 tablespoonful (7.5 mL) 6 years of age                                      every 4 hoursChildren under 2 years of age                Consult your doctor

Which are Bisolvine Child UNII Codes?

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

Which are Bisolvine Child 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:

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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".