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FDA Registration for Antacid Drug Products

Antacid drug products are regulated as OTC Monograph drugs by FDA. Active ingredients include calcium carbonate, magnesium hydroxide, aluminum hydroxide, and sodium bicarbonate.

OTC MonographDrug Facts Labeling21 CFR Part 207Since 2009

FDA Requirements for Antacid Drug Products

Antacid drug products are regulated as OTC drugs. Active ingredients in OTC antacids include calcium carbonate, magnesium hydroxide, aluminum hydroxide, magnesium oxide, and sodium bicarbonate.

All antacid manufacturers must register with FDA as drug establishments, obtain an NDC labeler code, and list each product with Drug Facts labeling.

  • FDA Drug Establishment Registration
  • NDC Labeler Code — required for all antacid products
  • Drug Listing in SPL format with Drug Facts panel
  • Annual renewal required October 1–December 31
  • GMP compliance under 21 CFR Parts 210 & 211

Antacids are over-the-counter (OTC) monograph drugs, meaning they’ve been evaluated by the FDA for safety and effectiveness and are generally safe for self-care. Antacids relieve heartburn (indigestion). They work by changing the stomach acid that causes heartburn, acid indigestion, and upset stomach. However, antacids don’t address the root cause of these issues and shouldn’t be used for prolonged periods without consulting a doctor.

Active Ingredients OTC Monograph Number
Basic aluminum carbonate gel M001.11 (Part 331)
Aluminum hydroxide M001.11 (Part 331)
Dihydroxyaluminum aminoacetate and dihydroxyaluminum aminoacetic acid M001.11 (Part 331)
Aluminum phosphate gel when used as part of an antacid combination product and contributing at least 25 percent of the total acid-neutralizing capacity; maximum daily dosage limit is 8 grams. M001.11 (Part 331)
Dihydroxyaluminum sodium carbonate M001.11 (Part 331)
Bicarbonate-containing active ingredients: Bicarbonate ion M001.11 (Part 331)
Bismuth aluminate M001.11 (Part 331)
Bismuth carbonate M001.11 (Part 331)
Bismuth subcarbonate M001.11 (Part 331)
Bismuth subgallate M001.11 (Part 331)
Bismuth subnitrate M001.11 (Part 331)
Calcium-containing active ingredients (Calcium, as carbonate or phosphate; maximum daily dosage limit 160 mEq calcium) M001.11 (Part 331)
Citrate-containing active ingredients (Citrate ion, as citric acid or salt; maximum daily dosage limit 8 grams.) M001.11 (Part 331)
Glycine (aminoacetic acid) M001.11 (Part 331)
Hydrate magnesium aluminate activated sulfate M001.11 (Part 331)
Magaldrate M001.11 (Part 331)
Magnesium aluminosilicates M001.11 (Part 331)
Magnesium carbonate M001.11 (Part 331)
Magnesium glycinate M001.11 (Part 331)
Magnesium hydroxide M001.11 (Part 331)
Magnesium oxide M001.11 (Part 331)
Magnesium trisilicate M001.11 (Part 331)
Milk solids, dried M001.11 (Part 331)
Aluminum phosphate M001.11 (Part 331)
Mono- or dibasic calcium salt M001.11 (Part 331)
Tricalcium phosphate M001.11 (Part 331)
Potassium bicarbonate (or carbonate when used as a component of an effervescent preparation) M001.11 (Part 331)
Sodium bicarbonate (or carbonate when used as a component of an effervescent preparation) M001.11 (Part 331)
Sodium potassium tartrate M001.11 (Part 331)
Magnesium aluminosilicates M001.11 (Part 331)
Magnesium trisilicate M001.11 (Part 331)
Tartrate-containing active ingredients (Tartaric acid or its salts; maximum daily dosage limit 200 mEq (15 grams) of tartrate.) M001.11 (Part 331)

These are not complete list of ingredients in FDA OTC drug monograph. The status of ingredient in OTC monograph may change please contact FDA for updated information.

Antacid Drug Products — FAQs

Common questions about FDA registration requirements for antacid drug products.
Yes. All antacid products making drug claims (e.g., relieves heartburn, acid indigestion) are regulated as OTC drugs.
Drug establishment registration, NDC labeler code, and drug listing are required before marketing antacids in the USA.
Yes, if the manufacturing establishment is outside the United States.

Ready to Register Your Antacid Drug Products?

LMG handles drug establishment registration, OTC drug listing, and NDC labeler code for antacid drug products manufacturers worldwide.

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