SUPREME ANTACID- calcium carbonate, magnesium hydroxide liquid

Supreme Antacid by

Drug Labeling and Warnings

Supreme Antacid by is a Otc medication manufactured, distributed, or labeled by H E B, Guardian Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each 10 mL )

Calcium carbonate 800 mg
Magnesium hydroxide 270 mg

PURPOSE

Antacid
Antacid

USE(S)

relieves:

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

WARNINGS

Do not take more than 60 mL in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

ASK A DOCTOR BEFORE USE IF YOU HAVE

• kidney disease
• a magnesium-restricted diet

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE 

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

STOP USE AND ASK DOCTOR

if symptoms last more than two weeks

KEEP OUT OF REACH OF CHILDREN

In case of overdose get medical help or contact a Poison Control Center immediately.

DIRECTIONS

• shake well before use
• mL = milliliter
• adults and children 12 years and older: take 10 to 20 mL two times a day, or as directed by a doctor
• children under 12 years: consult a doctor

OTHER INFORMATION

• each 10 mL contains: calcium 320 mg, magnesium 120 mg, sodium 10 mg
• store at controlled room temperature 20ºC-25ºC (68º-77ºF)
• do not freeze

INACTIVE INGREDIENTS

benzyl alcohol, flavor, hydroxyethyl cellulose, purified water, saccharin sodium, simethicone, sodium carbonate, sorbitol, xanthan gum.

Questions or comments?

1-(609) 860-2600 Mon.- Fri. 8:00 am - 4:30 pm

PRINCIPAL DISPLAY PANEL

NDC: 37808-614-05

H-E-B®

 

Supreme
Antacid

Calcium Carbonate, 800 mg

Magnesium Hydroxide, 270 mg

Antacid

 

Relief of:

• Acid Indigestion
• Heartburn
• Sour Stomach
• Upset Stomach
  
  

Cherry Creme

12 FL OZ (355 mL)

INGREDIENTS AND APPEARANCE

SUPREME ANTACID 
calcium carbonate, magnesium hydroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-614
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P)	MAGNESIUM HYDROXIDE	270 mg  in 10 mL
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	800 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM CARBONATE (UNII: 45P3261C7T)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-614-05	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/07/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	02/07/2025

Labeler - H E B (007924756)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	MANUFACTURE(37808-614)