SODIUM BICARBONATE- sodium bicarbonate powder 
Pharma Nobis, LLC

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Private Label Sodium Bicarbonate


Drug Facts

Active Ingredient

Soduim Bicarbonate, USP

Purpose

Antacid

Use

For relief of heartburn, acid indigestion, and upset stomach associated with these symptoms.

Warnings
NOT FOR INJECTIONS

Except under supervision of a doctor do not administer to children under 6 years of age.

Do not take more than six, 1/2 tsp. per person up to 60 years old, or three 1/2 tsp. per person 60 years or older in a 24 hour period.

Do not use this product if you are on a sodium restricted diet (each 1/2 tsp. contains 30 mEq (0.7 g) Sodium).

Do not use the maximum does more than 2 weeks.

Ask a doctor or pharmacist before use if

you are currently taking a prescription drug. Antacids may interact with certain prescription drugs.

Keep out of reach of children.

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

Directions

Adult and children 6 yrs of age and older:

Take 1/2 tsp. in 1/2 g;ass (4 fl oz) of water every 2 hrs. up to maximum dosage or as directed by doctor.

Inactive ingredients

none

Premier Value Label

4 oz

PV 4

16 oz

PV 16

Vida Mia Label

VM

Medis Label

Medis NaBicarb.jpg

SODIUM BICARBONATE 
sodium bicarbonate powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82645-904
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE1000 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82645-904-01454 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/27/2017
2NDC:82645-904-94113 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/27/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00110/27/2017
Labeler - Pharma Nobis, LLC (118564114)
Registrant - Pharma Nobis, LLC (118564114)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Nobis, LLC118564114label(82645-904) , manufacture(82645-904) , pack(82645-904) , analysis(82645-904)

Revised: 12/2023
Document Id: 0d1ce47a-8aa6-6673-e063-6294a90a9456
Set id: e42f674b-1a70-6a3c-e053-2995a90afa72
Version: 2
Effective Time: 20231222
 
Pharma Nobis, LLC