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Maximum strength gas relief - Medication Information

Product NDC Code 63868-975
Drug Name

Maximum strength gas relief

Type Brand
Pharm Class Skin Barrier Activity [PE]
Active Ingredients
Dimethicone 250 mg/1
Route ORAL
Dosage Form CAPSULE, LIQUID FILLED
RxCUI drug identifier 412111
Application Number part332
Labeler Name Chain Drug Marketing Association, Inc.
Packages
Package NDC Code Description
63868-975-06 1 bottle, plastic in 1 carton (63868-975-06) / 60 capsule, liquid filled in 1 bottle, plastic
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each softgel) Simethicone 250 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Swallow one or two softgels as symptoms occur do not exceed 2 softgels per 24 hours except under the advice and supervision of a physician

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients D&C red #33, edible ink, FD&C blue #1, gelatin, glycerin, peppermint oil, purified water

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses relieves bloating, pressure or fullness commonly referred to as gas

Purpose

Information about the drug product’s indications for use.
Purpose Anti-gas

Spl product data elements

Usually a list of ingredients in a drug product.
Maximum Strength Gas Relief Simethicone DIMETHICONE DIMETHICONE D&C RED NO. 33 FD&C BLUE NO. 1 GELATIN, UNSPECIFIED GLYCERIN PEPPERMINT OIL WATER oblong 813

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Packaging MSGasRelf1

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts QUALITY CHOICE *Compare to the active Ingredient in Maximum Strength Phazyme ® TAMPER EVIDENT: DO NOT USE IF PRINTED SEAL UNDER CAP IS CUT TORN OR MISSING *This product is not manufactured or distributed by C.B. Fleet Company Inc., distributor of PHAZYME ® . Product of UAE Packaged and Qualify Assured in the USA REV.01-092022 QC 100% SATISFACTION GUARANTEED Distributed by CDMA, Inc. Novi, MI 48375 www.qualitychoice.com Questions: 800-935-2362

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep ​out of reach of children.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-888-577-8033

Storage and handling

Information about safe storage and handling of the drug product.
Other information store at room temperature 20-25°C (68-77°F) protect from heat, humidity and light

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Stop use and ask a doctor if condition persists If pregnant or breast-feeding, ask a health professional before use. Keep ​out of reach of children.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API