DRxCHOICE Simethicone Gas Relief 36 Chewable Tablets

Manufacturer: Raritan Pharmaceuticals Inc
Effective date: 2026-09-08
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: daily-update
Hydrated at: 2026-09-11 03:01:24

Label at a glance#

ProductGas Relief Mint Flavor

Active ingredientDIMETHICONE, UNSPECIFIED

Label structure8 sections

Indications and uses

Relieves: • bloating • pressure • symptoms referred to as gas

Dosage and administration

• thoroughly chew 1 to 2 tablets as needed after meals and at bedtime • do not exceed 4 tablets in 24 hours period except under the advice and supervision of a physician.

Storage and handling

• store at room temperature 20-25ºC (68-77ºF) • each tablets contains: calcium 60mg

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Simethicone 80 mg

Purpose

OTC - PURPOSE SECTION

Antigas

Uses

INDICATIONS & USAGE SECTION

Relieves:

bloating
pressure
symptoms referred to as gas

Warnings

WARNINGS SECTION

Keep out of reach of children.In case of overdose, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

thoroughly chew 1 to 2 tablets as needed after meals and at bedtime
do not exceed 4 tablets in 24 hours period except under the advice and supervision of a physician.

Other information

STORAGE AND HANDLING SECTION

store at room temperature 20-25ºC (68-77ºF)
each tablets contains: calcium 60mg

Inactive ingredients

INACTIVE INGREDIENT SECTION

dextrose, peppermint flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, silica, tribasic calcium phosphate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 68163-111-36

DRx CHOICE

Gas Relief

Anti Gas/Simethicone 80 mg

For fast relief of Bloating, Pressure & Gas Distress

Mint Flavor

Naturally and Artificially Flavored

36 CHEWABLE TABLETS

Manufactured by: Raritan Pharmaceuticals

8 Joanna Court, East Brunswick, NJ 08816

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68163-111-36	EA - Each	68163-111	e4bc9f7a-7ff0-41e3-bd04-38878acb893c	1	2024-05-16

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

Gas Relief Mint Flavor
Simethicone
DIMETHICONE, UNSPECIFIED
DEXTROSE, UNSPECIFIED FORM
PEPPERMINT
MAGNESIUM STEARATE
MALTODEXTRIN
MICROCRYSTALLINE CELLULOSE
SILICON DIOXIDE
TRICALCIUM PHOSPHATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68163-111	68163-111-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIMETHICONE, UNSPECIFIED	92RU3N3Y1O	ACTIB
DEXTROSE, UNSPECIFIED FORM	IY9XDZ35W2	IACT
PEPPERMINT	V95R5KMY2B	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
TRICALCIUM PHOSPHATE	K4C08XP666	IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
7	2025-09-26	full-release	2026-06-01 01:14:55

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gas Relief Mint Flavor	SIMETHICONE	Raritan Pharmaceuticals Inc	329388cb-3ca1-4ecb-8b50-b1f9e0052559	2026-09-08	Warnings	Exact identifier ndc (package): 68163-111-36 ndc (product): 68163-111 ndc11 (package): 68163011136 spl id: 7e90e3f2-4ee2-4765-b719-90770ae673e7 spl set id: 329388cb-3ca1-4ecb-8b50-b1f9e0052559

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.