Medis Sodium Bicarbonate Powder
FDA Label NDC 0802-2685

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Humco Holding Group, Inc for the product Medis Sodium Bicarbonate (NDC 0802-2685). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings not for injections, ask a doctor or pharmacist before use if, keep out of reach of children., directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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

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