Heartburn Relief to Go

Dosage form: powder
Ingredients: Calcium carbonate 1000mg
Labeler: Breakthrough Products Inc.
NDC Code: 51596-005

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Urgent-Rx®
Heartburn
Relief to Go

Drug Facts

Active ingredient (per powder)

Calcium carbonate 1000mg

Purpose

Antacid

Uses

relieves

  • heartburn
  • sour stomach
  • acid indigestion
  • upset stomach associated with these symptoms

Warnings

Ask a doctor or pharmacist before use if you are take a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

  • do not take more than 8 powders in 24 hours
  • do not use the maximum dosage for more than 2 weeks.

Keep out of reach of children.

Directions
  • see instructions above for opening packet
  • place 1 powder on the tongue and swallow with or without water as symptoms occur, or as directed by a doctor

Inactive ingredients

flavor, sucralose

Questions?

1-888-99-URGENT (Mon-Fri 9AM-5PM MDT)

Do not use if pouch
is torn or open

distributed by
URGENT Rx®
Breakthrough Products, Inc.
Denver, CO 80202

PRINCIPAL DISPLAY PANEL - Pouch Label

New!

RIGHT
NOW
RELIEF

No Liquid Required
FAST POWDERS™
Pour Directly In Mouth

SEE OPENING INSTRUCTIONS ON BACK PANEL

HEART
BURN

URGENT Rx®

RELIEF
TO-GO

CALCIUM CARBONATE / ANTACID

mixed berry

distributed by UrgentRx

1 POWDER PACK

HEARTBURN RELIEF TO GO 
calcium carbonate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51596-005
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Calcium carbonate (carbonate ion) Calcium carbonate1000 mg
Inactive Ingredients
Ingredient NameStrength
sucralose 
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorBERRY (Mixed berry) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:51596-005-055 POUCH in 1 BOX
1NDC:51596-005-011 POWDER in 1 POUCH
2NDC:51596-005-1212 POUCH in 1 BOX
2NDC:51596-005-011 POWDER in 1 POUCH
3NDC:51596-005-2424 POUCH in 1 BOX
3NDC:51596-005-011 POWDER in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33109/01/2011
Labeler - Breakthrough Products Inc. (962008251)

Revised: 11/2013
 
Breakthrough Products Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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