SODIUM BICARBONATE 10 GR (650 MG)- sodium bicarbonate tablet 
Unity Pharma

----------

Sodium Bicarbonate Tablets, USP 10gr (650 mg)

Drug Facts

Active ingredient (in each tablet)

Sodium Bicarbonate 10 gr (650 mg)

Purpose

Antacid

Uses

relieves:

Warnings

Do not takemore than 24 tablets for adults up to 60 years of age (or 12 tablets for adults 60 years of age and older) in a 24-hour period nor use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician.

Ask a doctor before use if you havea sodium restricted diet.

Ask a doctor or pharmacist before use if you aretaking a prescription drug.

Antacids may interact with certain prescription drugs.

Stop use and ask a doctor ifsymptoms last more than 2 weeks.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

Directions

Other information

each tablet contains: sodium 178 mg (7.74 mEq)

store at room temperature 15º - 30º C (59º - 86º F) in a well closed container as defined in the USP

Inactive ingredients

Microcrystalline cellulose and stearic acid

Questions or comments?

1-833-687-7786

Manufactured for and Distributed By:

Unity Pharma

Covina, Ca 91723 USA

Rev. 09/24

Unity Pharma

NDC: 84275-503-10

Sodium Bicarbonate Tablets, USP 10 gr (650 mg)

ANTACID

1000 Tablets

sod-bicar-unity

SODIUM BICARBONATE  10 GR (650 MG)
sodium bicarbonate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84275-503
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE650 mg
Inactive Ingredients
Ingredient NameStrength
STEARIC ACID (UNII: 4ELV7Z65AP)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize10mm
FlavorImprint Code S65
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84275-503-101000 in 1 BOTTLE; Type 0: Not a Combination Product11/13/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00111/13/2024
Labeler - Unity Pharma (116124438)
Establishment
NameAddressID/FEIBusiness Operations
Neeyaan LLC118819217manufacture(84275-503)

Revised: 11/2024
Document Id: 2734de9d-d5ef-b3aa-e063-6394a90a60bf
Set id: 26d28a16-43bc-6db8-e063-6394a90a9230
Version: 2
Effective Time: 20241118
 
Unity Pharma