NDC 49035-306 Equate Clear Lax

Polyethylene Glycol 3350 Powder, For Solution Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
49035-306
Proprietary Name:
Equate Clear Lax
Non-Proprietary Name: [1]
Polyethylene Glycol 3350
Substance Name: [2]
Polyethylene Glycol 3350
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Wal-mart Stores Inc
    Labeler Code:
    49035
    FDA Application Number: [6]
    ANDA090685
    Marketing Category: [8]
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date: [9]
    10-08-2009
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Product Characteristics

    Color(s):
    WHITE (C48325)

    Product Packages

    NDC Code 49035-306-01

    Package Description: 119 g in 1 BOTTLE

    NDC Code 49035-306-02

    Package Description: 238 g in 1 BOTTLE

    NDC Code 49035-306-03

    Package Description: 510 g in 1 BOTTLE

    NDC Code 49035-306-09

    Package Description: 765 g in 1 BOTTLE

    Product Details

    What is NDC 49035-306?

    The NDC code 49035-306 is assigned by the FDA to the product Equate Clear Lax which is a human over the counter drug product labeled by Wal-mart Stores Inc. The generic name of Equate Clear Lax is polyethylene glycol 3350. The product's dosage form is powder, for solution and is administered via oral form. The product is distributed in 4 packages with assigned NDC codes 49035-306-01 119 g in 1 bottle , 49035-306-02 238 g in 1 bottle , 49035-306-03 510 g in 1 bottle , 49035-306-09 765 g 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 Equate Clear Lax?

    This medication is used to treat occasional constipation. It works by holding water in the stool to soften the stool and increases the number of bowel movements. It is known as an osmotic-type laxative. This medication is also available without a prescription. If you are taking this medication for self-treatment, it is important to read the manufacturer's package instructions carefully so you know when to consult your doctor or pharmacist. (See also Precautions.)

    What are Equate Clear Lax Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    Which are Equate Clear Lax UNII Codes?

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

    • POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
    • POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) (Active Moiety)

    What is the NDC to RxNorm Crosswalk for Equate Clear Lax?

    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: 876193 - polyethylene glycol 3350 17 GM Powder for Oral Solution
    • RxCUI: 876193 - polyethylene glycol 3350 17000 MG Powder for Oral Solution
    • RxCUI: 880407 - ClearLax 17 GM Powder for Oral Solution
    • RxCUI: 880407 - polyethylene glycol 3350 17000 MG Powder for Oral Solution [ClearLax]

    Which are the Pharmacologic Classes for Equate Clear Lax?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Patient Education

    Polyethylene Glycol 3350


    Polyethylene glycol 3350 is used to treat occasional constipation. Polyethylene glycol 3350 is in a class of medications called osmotic laxatives. It works by causing water to be retained with the stool. This increases the number of bowel movements and softens the stool so it is easier to pass.
    [Learn More]


    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [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".