GAS RELIEF EXTRA STRENGTH- simethicone capsule, liquid filled 
P & L Development, LLC

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Drug Facts

Active ingredient (in each softgel)

Simethicone 125 mg

Purpose

Antigas

Uses

for the relief of pressure, bloating, and fullness commonly referred to as gas.

Warnings

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Directions

Other information

Inactive ingredients

D&C yellow #10, edible ink, FD&C blue #1, FD&C red #40, gelatin, glycerin, mannitol, peppermint oil, purified water, sorbitan, sorbitol, titanium dioxide


Questions or comments?

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

Principal Display Panel

Compare to the active ingredient in Gas-X® Extra Strength†

extra strength

gas relief

simethicone 125 mg

anti-gas

Relieves:

softgels

†This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Gas-X® Extra Strength.

TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

Distributed by:

PL Developments

200 Hicks Street

Westbury, NY 11590

Product Label

Simethicone 125 mg

READYinCASE Extra Strength Gas Relief

GAS RELIEF  EXTRA STRENGTH
simethicone capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59726-897
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE125 mg
Inactive Ingredients
Ingredient NameStrength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
WATER (UNII: 059QF0KO0R)  
SORBITAN (UNII: 6O92ICV9RU)  
SORBITOL (UNII: 506T60A25R)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
MANNITOL (UNII: 3OWL53L36A)  
Product Characteristics
ColorgreenScoreno score
ShapeOVALSize9mm
FlavorImprint Code PO
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59726-897-1010 in 1 CARTON07/31/2019
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:59726-897-51150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/31/2019
3NDC:59726-897-1515 in 1 CARTON07/31/2019
31 in 1 BLISTER PACK; Type 0: Not a Combination Product
4NDC:59726-897-5050 in 1 CARTON07/31/2019
41 in 1 BLISTER PACK; Type 0: Not a Combination Product
5NDC:59726-897-3030 in 1 CARTON07/31/2019
51 in 1 BLISTER PACK; Type 0: Not a Combination Product
6NDC:59726-897-2020 in 1 CARTON07/31/2019
61 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01607/31/2019
Labeler - P & L Development, LLC (800014821)

Revised: 4/2024
Document Id: 0309c566-4379-4911-8b6c-e612c2a9ed6f
Set id: 4120832d-6c98-43f6-bdac-c88376c88c30
Version: 6
Effective Time: 20240430
 
P & L Development, LLC