NDC 49035-906 Mix-in Laxative Packets

Polyethylene Glycol 3350

NDC Product Code 49035-906

NDC CODE: 49035-906

Proprietary Name: Mix-in Laxative Packets What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Polyethylene Glycol 3350 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • 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.)

NDC Code Structure

  • 49035 - Wal-mart Stores Inc

NDC 49035-906-03

Package Description: 10 PACKET in 1 CARTON > 17 g in 1 PACKET

NDC Product Information

Mix-in Laxative Packets with NDC 49035-906 is a a human over the counter drug product labeled by Wal-mart Stores Inc. The generic name of Mix-in Laxative Packets is polyethylene glycol 3350. The product's dosage form is powder, for solution and is administered via oral form.

Labeler Name: Wal-mart Stores Inc

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.

Product Type: Human Otc Drug 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.

Mix-in Laxative Packets Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • POLYETHYLENE GLYCOL 3350 17 g/17g

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Wal-mart Stores Inc
Labeler Code: 49035
FDA Application Number: ANDA203928 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.

Marketing Category: ANDA - A product marketed under an approved Abbreviated New Drug Application. 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.

Start Marketing Date: 10-28-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Mix-in Laxative Packets Product Label Images

Mix-in Laxative Packets Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (In Each Dose)

Polyethylene Glycol 3350, 17 g

Purpose

Osmotic Laxative

Use

  • Relieves occasional constipation (irregularity)generally produces a bowel movement in 1 to 3 days

Warnings

Allergy alert: Do not use if you are allergic to polyethylene glycol

Do Not Use

If you have kidney disease, except under the advice and supervision of a doctor

Ask A Doctor Before Use If You Have

  • Nausea, vomiting or abdominal paina sudden change in bowel habits that lasts over 2 weeksirritable bowel syndrome

Ask A Doctor Or Pharmacist Before Use If You Are

Taking a prescription drug

When Using This Product

You may have loose, watery, more frequent stools

Stop Use And Ask A Doctor If

  • You have rectal bleeding or your nausea, bloating, cramping or abdominal pain gets worse. These may be signs of a serious condition.you need to use a laxative for longer than 1 weekyou get diarrhea

If Pregnant Or Breast-Feeding,

Ask a health professional before use.

Keep Out Of Reach Of Children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • Do not take more than directed unless advised by your doctoradults and children 17 years of age and older:stir and dissolve one packet of powder (17 g) in any 4 to 8 ounces of beverage (cold, hot or room temperature) then drinkensure that the powder is fully dissolved before drinkingdo not drink if there are any clumpsuse once a dayuse no more than 7 dayschildren 16 years of age or under: ask a doctor

Other Information

  • Store at 20º to 25ºC (68º to 77ºF)tamper-evident: do not use if foil is open or broken

Inactive Ingredients

None

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