HEARTBURN RELIEF TO GO- calcium carbonate powder 
Breakthrough Products Inc.

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.

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Heartburn Relief to Go™

Drug Facts

Active ingredient (per powder)

Calcium carbonate 1000mg

Purpose

Antacid

Uses

Relieves:

Warnings

Ask a doctor or pharmacist before use if you are taking 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

Inactive ingredients

acacia gum, flavor, maltodextrin, sucralose

Questions?

1-888-998-7436 (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 - 1 Powder Packet

NO
WATER
REQUIRED
POUR DIRECTLY IN MOUTH

New!

URGENT Rx®
FAST
POWDERS™

◀ SEE OPENING INSTRUCTIONS ON BACK PANEL ▶

HEART
BURN
URGENT Rx®
RELIEF
TO-GO™

CALCIUM CARBONATE/
ANTACID

mixed berry

distributed by UrgentRx

1 POWDER PACK

PRINCIPAL DISPLAY PANEL - 1 Powder Packet
HEARTBURN RELIEF TO GO 
calcium carbonate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51596-005
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Calcium carbonate (UNII: H0G9379FGK) (carbonate ion - UNII:7UJQ5OPE7D) Calcium carbonate1000 mg
Inactive Ingredients
Ingredient NameStrength
acacia (UNII: 5C5403N26O)  
maltodextrin (UNII: 7CVR7L4A2D)  
sucralose (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorBERRY (Mixed berry) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51596-005-1010 in 1 BOX
11 in 1 PACKET; Type 0: Not a Combination Product
2NDC:51596-005-055 in 1 BOX
2NDC:51596-005-011 in 1 POUCH; Type 0: Not a Combination Product
3NDC:51596-005-1212 in 1 BOX
3NDC:51596-005-011 in 1 POUCH; Type 0: Not a Combination Product
4NDC:51596-005-2424 in 1 BOX
4NDC:51596-005-011 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33109/01/2011
Labeler - Breakthrough Products Inc. (962008251)

Revised: 10/2014
Document Id: f967a69f-b048-4776-a0b9-11562d5a1c29
Set id: 88cadd90-c6f4-4229-aed4-bf3e4ce6dbf5
Version: 3
Effective Time: 20141006
 
Breakthrough Products Inc.