CURIST GAS RELIEF MAXIMUM STRENGTH- simethicone capsule, liquid filled

Curist Gas Relief by

Drug Labeling and Warnings

Curist Gas Relief by is a Otc medication manufactured, distributed, or labeled by Little Pharma, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient (in each softgel)

Simethicone 250 mg

PURPOSE

Purpose

Antigas

INDICATIONS & USAGE

Use

Relieves pressure, bloating, or fullness commonly referred to as gas

WARNINGS

Warnings

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

• Swallow 1 or 2 softgels with at least 8 oz of water, as needed after a meal or at bedtime.
• Do not exceed 2 softgels in 24 hours except under the advice and supervision of a physician.

STORAGE AND HANDLING

Other information

Store at room temperature 20-25°C (68-77°F)

INACTIVE INGREDIENT

Inactive ingredients D&C red #33, FD&C blue #1, gelatin, glycerin, and purified water

QUESTIONS

Questions or comments? 1-844-243-1241 Monday - Friday 9AM - 5PM EST

SPL UNCLASSIFIED SECTION

Distributed by:
Little Pharma, Inc.
New York, NY 10023

Made in Canada

PRINCIPAL DISPLAY PANEL

curist

Gas Relief Maximum Strength

Simethicone 250 mg

Anti-Gas

Fast Relief of Gas Pressure, Bloating, and Discomfort

300 Softgels

INGREDIENTS AND APPEARANCE

CURIST GAS RELIEF  MAXIMUM STRENGTH
simethicone capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72559-019
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	250 mg

Inactive Ingredients
Ingredient Name	Strength
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Product Characteristics
Color	purple (Clear purple)	Score	no score
Shape	OVAL	Size	13mm
Flavor		Imprint Code	250
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72559-019-23	300 in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M002	04/07/2022

Labeler - Little Pharma, Inc. (074328189)