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  4. NDC Product Code: 66594-333 Pro-clear AC

NDC 66594-333 Pro-clear AC

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66594-333?
  5. Pro-clear AC Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66594-333
Proprietary Name:
Pro-clear AC
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pro-pharma Llc
Labeler Code:
66594
Product Label ID:
8a76d7e5-e8ae-48e4-879d-6c8e3789bd26
Start Marketing Date: [9]
09-08-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
COTTON CANDY (C73382)

Code Structure Chart

Product Details

What is NDC 66594-333?

The NDC code 66594-333 is assigned by the FDA to the product Pro-clear AC 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 66594-333-01 30 ml in 1 bottle , 66594-333-16 473 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-clear AC?

Do not exceed recommended dosage.Adults andchildren 12years of ageand over:2 teaspoonfuls (10 mL)every 4 hours, not toexceed 6 doses in 24 hours.Children 6to under 12years of age:1 teaspoonful (5 mL)every 4 hours, not to exceed 6 doses in 24 hoursChildrenunder 6years of age:Consult a doctor.A special measuring device should be used to give an accurate dose of this product to children under 6 years of age.  Giving a higher dose than recommended by a doctor could result in serious side effects for your child.

Which are Pro-clear AC UNII Codes?

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

Which are Pro-clear AC 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-clear AC?

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: 995447 - codeine phosphate 9 MG / pyrilamine maleate 8.33 MG in 5 mL Oral Solution
  • RxCUI: 995447 - codeine phosphate 1.8 MG/ML / pyrilamine maleate 1.67 MG/ML Oral Solution
  • RxCUI: 995447 - codeine phosphate 9 MG / pyrilamine maleate 8.33 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".