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Gas relief ultra strength - Medication Information

Product NDC Code 41250-343
Drug Name

Gas relief ultra strength

Type Brand
Pharm Class Skin Barrier Activity [PE]
Active Ingredients
Dimethicone 180 mg/1
Route ORAL
Dosage Form CAPSULE, LIQUID FILLED
RxCUI drug identifier 252294
Application Number part332
Labeler Name MEIJER, INC.
Packages
Package NDC Code Description
41250-343-50 50 blister pack in 1 carton (41250-343-50) / 1 capsule, liquid filled in 1 blister pack
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each softgel) Simethicone 180 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 adult: swallow with water 1 or 2 softgels as needed after meal and at bedtime do not exceed 2 softgels in 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 FD&C red #40*, FD&C yellow # 6, gelatin, glycerin, purified water, white printing ink* *contains one or more of these ingredients

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 For the relief of pressure and bloating commonly referred to as gas.

Purpose

Information about the drug product’s indications for use.
Purpose Antigas

Spl product data elements

Usually a list of ingredients in a drug product.
Gas Relief Ultra Strength Simethicone DIMETHICONE DIMETHICONE FD&C YELLOW NO. 6 GELATIN GLYCERIN WATER FD&C RED NO. 40 S180;05A

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.
Principal Display Panel Compare to Gas-X Ultra Strength active ingredient† ULTRA STRENGTH gas relief Simethicone | 180 mg FAST RELIEF OF: Gas, Pressure, Bloating, Discomfort Softgels SMALL, EASY TO SWALLOW †This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Gas-X® Ultra Strength. TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN, OR SHOW ANY SIGNS OF TAMPERING. KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION. DIST. BY MEIJER DISTRIBUTION, INC. GRAND RAPID, MI 49544 www.meijer.com Package Label MEIJER Ultra Strength Gas Relief Simethicone 180 mg

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? Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health care professional before use.

Storage and handling

Information about safe storage and handling of the drug product.
Other information store between 15-30ºC (59º-86ºF) protect from heat and moisture

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 If pregnant or breast-feeding, ask a health care 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