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  4. NDC Product Code: 50090-1447 Sunmark Clearlax

NDC 50090-1447 Sunmark Clearlax

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50090-1447?
  5. Sunmark Clearlax Uses
  6. Active Ingredients UNII Codes
  7. 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:
50090-1447
Proprietary Name:
Sunmark Clearlax
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A-s Medication Solutions
Labeler Code:
50090
Product Label ID:
ac87ef10-1a56-4f0d-9c00-775095e96074
Start Marketing Date: [9]
10-07-2009
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 50090-1447-0

Package Description: 238 g in 1 BOTTLE

Product Details

What is NDC 50090-1447?

The NDC code 50090-1447 is assigned by the FDA to the product Sunmark Clearlax which is product labeled by A-s Medication Solutions. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50090-1447-0 238 g 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 Sunmark Clearlax?

•do not take more than directed unless advised by your doctor•the bottle top is a measuring cap marked to contain 17 grams of powder when filled to the indicated line (white section in cap)•adults and children 17 years of age and older:•fill to top of white section in cap which is marked to indicate the correct dose (17 g)•stir and dissolve in any 4 to 8 ounces of beverage (cold, hot or room temperature) then drink•use once a day•use no more than 7 days•children 16 years of age or under: ask a doctor

Which are Sunmark Clearlax UNII Codes?

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

  • POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
  • POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) (Active Moiety)

What is the NDC to RxNorm Crosswalk for Sunmark Clearlax?

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: 876193 - polyethylene glycol 3350 17 GM Powder for Oral Solution
  • RxCUI: 876193 - polyethylene glycol 3350 17000 MG Powder for Oral Solution
  • RxCUI: 880407 - ClearLax 17 GM Powder for Oral Solution
  • RxCUI: 880407 - polyethylene glycol 3350 17000 MG Powder for Oral Solution [ClearLax]

* 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".