NDC 66594-321 Pro-chlo

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:
66594-321
Proprietary Name:
Pro-chlo
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pro-pharma, Llc
Labeler Code:
66594
Start Marketing Date: [9]
12-12-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
COTTON CANDY (C73382)

Product Packages

NDC Code 66594-321-01

Package Description: 30 mL in 1 BOTTLE

NDC Code 66594-321-16

Package Description: 473 mL in 1 BOTTLE

Product Details

What is NDC 66594-321?

The NDC code 66594-321 is assigned by the FDA to the product Pro-chlo which is product labeled by Pro-pharma, Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 66594-321-01 30 ml in 1 bottle , 66594-321-16 473 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 Pro-chlo?

Do not exceed recommended dosage.Adults and children 12years of ageand over:2 teaspoonfuls (10 mL)every 6 hours, not toexceed 8 teaspoonfuls in24 hoursChildren 6 tounder 12 yearsof age:1 teaspoonful (5 mL)every 6 hours, not toexceed 4 teaspoonfuls in24 hoursChildren under6 years of age:Consult a doctor.

Which are Pro-chlo UNII Codes?

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

Which are Pro-chlo 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 Pro-chlo?

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: 1192685 - chlophedianol HCl 12.5 MG / phenylephrine HCl 5 MG / pyrilamine maleate 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1192685 - chlophedianol hydrochloride 2.5 MG/ML / phenylephrine hydrochloride 1 MG/ML / pyrilamine maleate 2.5 MG/ML Oral Solution
  • RxCUI: 1192685 - chlophedianol hydrochloride 12.5 MG / phenylephrine hydrochloride 5 MG / pyrilamine maleate 12.5 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".