ACID GONE ANTACID- aluminum hydroxide and magnesium carbonate liquid

ACID GONE ANTACID by

Drug Labeling and Warnings

ACID GONE ANTACID by is a Otc medication manufactured, distributed, or labeled by Major Pharmaceuticals, GCP Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each 15mL tablespoonful)

Aluminum hydroxide 95mg

Magnesium carbonate 358mg

Purpose

Antacid

Uses

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-restricted diet
• a sodium-restricted diet

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

• do not take more than 8 tablespoonfuls in 24 hours
• do not use the maximum dosage for more than 2 weeks
• laxative effect may occur

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

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

• shake well before use
• adults and children 12 years and older: take 1 to 2 tablespoonfuls four times a day or as directed by a doctor
• children under 12 years: ask a doctor
• take after meals and at bedtime
• dispense product only by spoon or other measuring device

Other information

• each 15 mL tablespoonful contains: magnesium 105mg, sodium 39mg
• store at up to 25°C (77°F)
• avoid freezing
• keep tightly closed
• TAMPER-EVIDENT: Do not use this product if inner foil seal over the mouth of the bottle is broken or missing.

Inactive ingredients (Regular Strength)

benzyl alcohol, D&C yellow #10, edetate disodium, FD&C blue #1, flavor, glycerin, purified water, saccharin sodium, sodium alginate, sorbitol solution, xanthan gum

Questions or comments?

1-800-540-3765

Principal Display Panel

major

NDC: 0904-7727-14

Acid Gone Antacid

Alumina and Magnesium Carbonate
Oral Suspension USP

Relieves Heartburn
& Acid Indigestion

Compare to the active ingredients in Gaviscon® *

12 FL OZ (355 mL)

INGREDIENTS AND APPEARANCE

ACID GONE ANTACID 
aluminum hydroxide and magnesium carbonate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0904-7727
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	95 mg  in 15 mL
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D)	MAGNESIUM CARBONATE	358 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
EDETATE DISODIUM (UNII: 7FLD91C86K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM ALGINATE (UNII: C269C4G2ZQ)
SORBITOL (UNII: 506T60A25R)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	green	Score
Shape		Size
Flavor	SPEARMINT (cool mint)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0904-7727-14	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	12/30/2004

Labeler - Major Pharmaceuticals (191427277)

Registrant - GCP Laboratories (965480861)

Establishment
Name	Address	ID/FEI	Business Operations
GCP Laboratories		965480861	manufacture(0904-7727)