SohMed Acid Reducer description, usages, side effects, indications, overdosage, supplying and lots more!

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SohMed Acid Reducer

SOHM Inc.

SohMed™ Acid Reducer


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients
(in each chewable tablet)
Purpose
Aluminum hydroxide 160 mg Antacid
Magnesium carbonate 105 mg Antacid

Use

relieves

  • heartburn
  • acid indigestion
  • sour stomach
  • upset stomach associated with these symptoms

Warnings

Ask a doctor before use if you have

  • kidney disease
  • a magnesium or sodium-restricted diet

Ask a doctor or pharmacist before use if you are now taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product do not take more than 16 tablets in a 24-hour period or use the maximum dosage for more than 2 weeks

Keep out of reach of children

Directions

  • chew 2 to 4 tablets four times a day or as directed by a doctor.
  • take after meals and at bedtime or as needed
  • for best results follow by a half glass of water or other liquid
  • do not swallow whole

SohMed Acid Reducer Other information

  • each tablet contains :
    magnesium 50 mg and sodium 32 mg
  • store at 20° -25°C.
  • See end flap for expiration date and lot number.

Inactive ingredients

alginic acid, calcium stearate, flavor, mannitol, sodium bicarbonate, starch, sucrose, water, FD&C Yellow # 5 (tartrazine), FD&C Yellow # 6, lactose, dextrose, talcum, sucralose

Question or comments ?

1 (856) 2863646

Distributed by : Sohm, Inc.
6920 Knott Ave., Suit A-C
Buena Park, CA 90621

PRINCIPAL DISPLAY PANEL - 50 Tablet Bottle Carton

NDC XXXXXXXXXXX

SohMed

*Compare to the active ingredients in Gaviscon® Extra Strength Antacid

Extra Strength

Acid Reducer Antacid

Aluminum Hydroxide 160 mg
Magnesium Carbonate 105 mg

Relieves Heartburn, Acid Indigestion and Sour Stomach

50 Tablets

Chewable Tablet

SohMed Acid Reducer

SohMed Acid Reducer

ALUMINUM HYDROXIDE and MAGNESIUM CARBONATE TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50405-002
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
aluminum hydroxide 160 mg
MAGNESIUM CARBONATE 105 mg

Inactive Ingredients

Ingredient Name Strength
ALGINIC ACID
CALCIUM STEARATE
mannitol
SODIUM BICARBONATE
STARCH, CORN
water
SUCROSE
FD&C YELLOW NO. 5
FD&C YELLOW NO. 6
LACTOSE
DEXTROSE
talc
Sucralose

Product Characteristics

Color Size Imprint Code Shape
YELLOW 18 mm CRX ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 50 in 1 BOTTLE, PLASTIC
2 NDC:50405-002-50 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2013-08-25


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Be sure to consult your doctor before taking any medication!
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