Pro-enema Single Saline Enema
NDC Package 71451-001-01
Package Information
Pro-enema Single Saline (sodium phosphate, dibasic and sodium phosphate, monobasic, unspecified form) enemas is a medication used as Active ingredients (in each 118mL delivered dose)PurposeDibasic Sodium Phosphate 7 gSaline laxativeMonobasic Sodium Phosphate 19 gSaline laxative. This formulation utilizes a enema delivery system. Marketed by Propharma Medical Supplies, this product is identified by NDC 71451-001 and is authorized under FDA application part334.
Identification & Billing
- RxCUI: 283100 - sodium phosphate, dibasic 7 GM / sodium phosphate, monobasic 19 GM in 118 ML Enema
- RxCUI: 283100 - sodium phosphate, dibasic 59.3 MG/ML / sodium phosphate, monobasic 161 MG/ML Enema
- RxCUI: 283100 - sodium phosphate, dibasic 3.5 GM / sodium phosphate, monobasic 9.5 GM per 59 ML Enema
- RxCUI: 283100 - sodium phosphate, dibasic 7 GM / sodium phosphate, monobasic 19 GM per 118 ML Enema
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 71451 - Propharma Medical Supplies
- 71451-001 - Pro-enema Single Saline
- 71451-001-01 - 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 133 mL in 1 BOTTLE, WITH APPLICATOR
- 71451-001 - Pro-enema Single Saline
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 71451-001-01 identifies a specific commercial package of 1 bottle, with applicator in 1 carton / 133 ml in 1 bottle, with applicator of Pro-enema Single Saline Laxative, a human over the counter drug labeled by Propharma Medical Supplies. This enema is formulated for rectal use and contains sodium phosphate, dibasic; sodium phosphate, monobasic, unspecified form 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 Propharma Medical Supplies on June 06, 2017. The current certification is valid through December 31, 2026.
How is this Propharma Medical Supplies product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 71451000101. 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.