NDC 0363-0127 Oral Saline Laxative

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:
0363-0127
Proprietary Name:
Oral Saline Laxative
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
0363
Start Marketing Date: [9]
10-05-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 0363-0127?

The NDC code 0363-0127 is assigned by the FDA to the product Oral Saline Laxative which is product labeled by Walgreen Co. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-0127-12 1 bottle in 1 carton / 45 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 Oral Saline Laxative?

•use as a laxative for relief of occasional constipation•dilute dose in the table below with one glass (8 fl. oz.) cool water. Drink, then follow with at least one additional glass (8 fl. oz.) cool water. There is significant loss of liquid when using this product. To prevent dehydration drink plenty of clear liquid after use.•Do not use for bowel cleansing.•Do not take more unless directed by a doctor. See Warning. There are three Teaspoons in one Tablespoon.Ages (Years)DosageMaximum Dose12 & Older3 Teaspoons6 or 9 Teaspoons*10 & 113 Teaspoons*3 Teaspoons*5 to 91 1/2 Teaspoons*1 1/2 Teaspoons*under 5Do Not UseDo Not Use *SINGLE DAILY DOSAGE. DO NOT TAKE MORE OF THIS PRODUCT IN A 24-HOUR PERIOD

Which are Oral Saline Laxative UNII Codes?

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

Which are Oral Saline Laxative 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 Oral Saline Laxative?

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: 1790675 - sodium phosphate, dibasic 1.4 GM / sodium phosphate, monobasic 6.2 GM in 15 mL Oral Solution
  • RxCUI: 1790675 - sodium phosphate, dibasic 93 MG/ML / sodium phosphate, monobasic 413 MG/ML Oral Solution
  • RxCUI: 1790675 - sodium phosphate, dibasic 1.4 GM / sodium phosphate, monobasic 6.2 GM per 15 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".