NDC 0904-7727 Acid Gone Antacid

Aluminum Hydroxide And Magnesium Carbonate

NDC Product Code 0904-7727

NDC CODE: 0904-7727

Proprietary Name: Acid Gone Antacid What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aluminum Hydroxide And Magnesium Carbonate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

GREEN (C48329)

NDC Code Structure

  • 0904 - Major Pharmaceuticals

NDC 0904-7727-14

Package Description: 355 mL in 1 BOTTLE

Price per Unit: $0.01049 per ML

NDC Product Information

Acid Gone Antacid with NDC 0904-7727 is a a human over the counter drug product labeled by Major Pharmaceuticals. The generic name of Acid Gone Antacid is aluminum hydroxide and magnesium carbonate. The product's dosage form is liquid and is administered via oral form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1251355 and 252203.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Acid Gone Antacid Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • SORBITOL (UNII: 506T60A25R)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Major Pharmaceuticals
Labeler Code: 0904
FDA Application Number: part331 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 12-30-2004 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Acid Gone Antacid Product Label Images

Acid Gone Antacid Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (In Each 15Ml Tablespoonful)

Aluminum hydroxide 95mgMagnesium carbonate 358mg




  • Relievesheartburnacid indigestionsour stomachupset stomach associated with these symptoms


  • Ask a doctor before use if you havekidney diseasea magnesium-restricted dieta sodium-restricted dietAsk a doctor or pharmacist before use if you are taking a prescription drug.
  • Antacids may interact with certain prescription drugs.
  • When using this productdo not take more than 8 tablespoonfuls in 24 hoursdo not use the maximum dosage for more than 2 weekslaxative effect may occurIf 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.


  • Shake well before useadults and children 12 years and older: take 1 to 2 tablespoonfuls four times a day or as directed by a doctorchildren under 12 years: ask a doctortake after meals and at bedtimedispense 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 freezingkeep tightly closedTAMPER-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

* Please review the disclaimer below.