NDC 17856-0771 Docu 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:
17856-0771
Proprietary Name:
Docu Liquid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corp.
Labeler Code:
17856
Start Marketing Date: [9]
08-01-1997
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Flavor(s):
VANILLA (C73421 - NATURAL AND ARTIFICIAL FLAVOR)

Product Packages

NDC Code 17856-0771-1

Package Description: 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 25 mL in 1 CUP, UNIT-DOSE

NDC Code 17856-0771-2

Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE

Product Details

What is NDC 17856-0771?

The NDC code 17856-0771 is assigned by the FDA to the product Docu Liquid which is product labeled by Atlantic Biologicals Corp.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 17856-0771-1 50 cup, unit-dose in 1 box, unit-dose / 25 ml in 1 cup, unit-dose, 17856-0771-2 72 cup, unit-dose in 1 box, unit-dose / 10 ml in 1 cup, unit-dose. 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 Docu Liquid?

•may be taken once daily or in divided doses•give dose in 1/2 glass of milk, fruit juice or infant formula to mask bitter taste and prevent throat irritationadults and children over 121 to 7 teaspoonschildren 2 to under 121 to 3 teaspoonschildren under 2ask a doctor

Which are Docu Liquid UNII Codes?

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

Which are Docu 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 Docu 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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Patient Education

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* 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".