Polyethylene Glycol 3350 Powder, For Solution
NDC Package 69230-324-39
Package Information
Polyethylene Glycol 3350 powders is (Bottle Only) • 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: • use once a day • 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 • do not combine with starch-based thickeners used for difficult swallowing • ensure that the powder is fully dissolved before drinking • do not drink if there are any clumps • do not use more than 7 days • children 16 years of age or under: ask a doctor (Packet Only) • do not take more than directed unless advised by your doctor • adults and children 17 years of age and older: • use once a day • stir and dissolve one packet of powder (17 g) in any 4 to 8 ounces of beverage (cold, hot or room temperature) then drink • do not combine with starch-based thickeners used for difficult swallowing • ensure that the powder is fully dissolved before drinking • do not drink if there are any clumps • do not use more than 7 days • children 16 years of age or under: ask a doctor. This formulation utilizes a powder, for solution delivery system. Marketed by Camber Consumer Care Inc, this product is identified by NDC 69230-324 and is authorized under FDA application ANDA214990.
Identification & Billing
- RxCUI: 876193 - polyethylene glycol 3350 17 GM Powder for Oral Solution
- RxCUI: 876193 - polyethylene glycol 3350 17000 MG Powder for Oral Solution
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69230 - Camber Consumer Care Inc
- 69230-324 - Polyethylene Glycol 3350
- 69230-324-39 - 765 g in 1 BOTTLE
- 69230-324 - Polyethylene Glycol 3350
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (69230-324). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 69230-324-39 identifies a specific commercial package of 765 g in 1 bottle of Polyethylene Glycol 3350, a human over the counter drug labeled by Camber Consumer Care Inc. This powder, for solution is formulated for oral use and contains polyethylene glycol 3350 as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Camber Consumer Care Inc on April 14, 2021. The current certification is valid through December 31, 2027.
How is this Camber Consumer Care Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69230032439. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.
