NDC 54868-6381 Biclora

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:
54868-6381
Proprietary Name:
Biclora
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Start Marketing Date: [9]
01-02-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 54868-6381-0

Package Description: 240 mL in 1 BOTTLE

Product Details

What is NDC 54868-6381?

The NDC code 54868-6381 is assigned by the FDA to the product Biclora which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54868-6381-0 240 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 Biclora?

Do not exceed recommended dosage.Use a calibrated measuring device for administering the drug to a child.Adults and children12 years of ageand over:2 teaspoonfuls (10 mL) every 6 to 8 hours,not to exceed 6 teaspoonfuls in 24 hours,or as directed by a doctor.Children 6 to under12 years of age:1 teaspoonful (5 mL) every 6 to 8 hours,not to exceed 3 teaspoonfuls in 24 hours,or as directed by a doctor.Children under 6 years of age:Consult a doctor.

Which are Biclora UNII Codes?

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

Which are Biclora 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 Biclora?

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: 1236710 - chlophedianol HCl 12.5 MG / chlorcyclizine HCl 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1236710 - chlophedianol hydrochloride 2.5 MG/ML / chlorcyclizine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1236710 - chlophedianol hydrochloride 12.5 MG / chlorcyclizine hydrochloride 12.5 MG per 5 ML Oral Solution
  • RxCUI: 1358165 - Biclora 12.5 MG / 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1358165 - chlophedianol hydrochloride 2.5 MG/ML / chlorcyclizine hydrochloride 2.5 MG/ML Oral Solution [Biclora]

* 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".