NDC 54162-195 Docusate Sodium Liquid

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:
54162-195
Proprietary Name:
Docusate Sodium Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Geritrex Llc
Labeler Code:
54162
Start Marketing Date: [9]
09-28-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54162-195-16

Package Description: 473 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 54162-195?

The NDC code 54162-195 is assigned by the FDA to the product Docusate Sodium Liquid which is product labeled by Geritrex Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54162-195-16 473 ml in 1 bottle, plastic . 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 Docusate Sodium Liquid?

Follow dosing directions below or take as directed by doctormust be given in a 6 to 8 oz glass of milk or fruit juice to prevent throat irritationmay be taken as a single daily dose or in divided dosestake maximum dose daily until first bowel movement, dosage should then be reduced according to individual responsedo not exceed recommended doseshake well before usingAdults and children 12 years and over1 to 6 teaspoons (50 to 300 mg)Children 2 to 12 years of age1 to 3 teaspoons (50 to 150 mg) 1 teaspoon = 5 mLTAMPER EVIDENT: Do not use if breakaway band on cap is broken or missing.Other informationStore at room temperature 15°-30°C (59°-86°F)protect from excessive heatKeep tightly closedDispense in tight, light resistant container as defined in the USPeach teaspoon (5 mL) contains: sodium 15 mg

Which are Docusate Sodium Liquid UNII Codes?

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

Which are Docusate Sodium Liquid 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 Docusate Sodium Liquid?

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:

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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".