RAPIDOL SODIUM BICARBONATE- sodium bicarbonate powder 
Pharmadel LLC

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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Rapidol Sodium Bicarbonate Antacid Powder (WP)

Drug Facts

Active Ingredient & Purposes

Active ingredient (in each ½ teaspoon) Purpose
Sodium bicarbonate 2,616 mg.........................................................................................................Antacid

Uses For the relief of an upset stomach associated with these symptoms

Warnings

Stomach Waring: To avoid serious injury, do not take powder until it is completely dissolved. It is very important not to take this product when overly full from food or drink. Consult a doctor if severe stomach pain occurs after taking this product.

Do not use

  • the maximum daily dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor
  • this product except under advice and supervision of a physician if you are allergic to milk or milk products

When using this product

  • may cause constipation
  • may have laxative effect

Ask a doctor or pharmacist before use if you are

  • presently taking a prescription drug. Antacids may interact with certain prescription drugs.

Ask a doctor before use if you have

  • a sodium-restricted diet

If pregnant or breast-feeding,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN.

In case of an accidental overdose, seek professional assistance or contact a Poison Control center right away.

Directions

agemaximum daily dosage
adults 60 years of age and over½ teaspoon, 3 times a day
adults under 60 and children 12 years of age and over½ teaspoon, 6 times a day
children under 12 years of agedo not use

Other information

None

Questions & comments?

PHARMADEL LLC.

New Castle, DE, 19720

+1-866-359-3478

www.pharmadel.com

Prinicpal Display Panel

55758-327-04

4 Oz

Rapidol SB 4 oz

RAPIDOL SODIUM BICARBONATE 
sodium bicarbonate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55758-319
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE2.6 g  in 2.6 g
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55758-319-04113 g in 1 BOTTLE; Type 0: Not a Combination Product11/23/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33111/23/2020
Labeler - Pharmadel LLC (030129680)

Revised: 3/2023
Document Id: b4c9a653-6f50-7c98-e053-2995a90ada37
Set id: b4c9a653-6f51-7c98-e053-2995a90ada37
Version: 1
Effective Time: 20230306
 
Pharmadel LLC