Acid Reducer
Omeprazole Magnesium · Tablet, Delayed Release · Oral
Active ingredient
Active ingredient (in each tablet) Famotidine 10 mg
Purpose
Purpose Acid reducer
Uses
Uses
• relieves heartburn associated with acid indigestion and sour stomach
• prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages
Warnings
Warnings Allergy alert: Do not use if you are allergic to famotidine or other acid reducers Do not use
• if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
• with other acid reducers Ask a doctor before use if you have
• had heartburn over 3 months. This may be a sign of a more serious condition.
• heartburn with lightheadedness, sweating, or dizziness
• chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
• frequent chest pain
• frequent wheezing, particularly with heartburn
• unexplained weight loss
• nausea or vomiting
• stomach pain
• kidney disease Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs. Stop use and ask a doctor if
• your heartburn continues or worsens
• you need to take this product for more than 14 days 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. (1-800-222-1222)
Do not use
Do not use
• if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
• with other acid reducers
Ask a doctor before use
Ask a doctor before use if you have
• had heartburn over 3 months. This may be a sign of a more serious condition.
• heartburn with lightheadedness, sweating, or dizziness
• chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
• frequent chest pain
• frequent wheezing, particularly with heartburn
• unexplained weight loss
• nausea or vomiting
• stomach pain
• kidney disease
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs.
Stop use and ask a doctor
Stop use and ask a doctor if
• your heartburn continues or worsens
• you need to take this product for more than 14 days
Pregnancy or breast-feeding
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
Directions
Directions
• adults and children 12 years and over:
• to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew.
• to prevent symptoms, swallow 1 tablet with a glass of water at any time from 15 to 60 minutes before eating food or drinking beverages that cause heartburn
• do not use more than 2 tablets in 24 hours
• children under 12 years: ask a doctor
Other information
Other information
• read the directions and warnings before use
• keep the carton. It contains important information.
• store at 20°-25°C (68°-77°F)
• protect from moisture
Inactive ingredients
Inactive ingredients carnauba wax, hypromellose, iron oxide red, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, pregelatinized starch, talc, titanium dioxide, triacetin
Questions?
Questions or comments? 1-800-719-9260
Label text from the FDA structured product label by Amazon.com Services LLC (revised Aug 31, 2026). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Omeprazole Magnesium in 20 products
- Famotidine in 14 products
- Esomeprazole Magnesium in 2 products
- Ranitidine Hydrochloride in 1 product
- Cimetidine in 1 product
Acid Reducer NDC products (38)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 10202-722 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | 7-Eleven | ANDA |
| 69168-443 | Famotidine 20 mg/1 Tablet | Allegiant Health | ANDA |
| 69168-445 | Famotidine 20 mg/1 Tablet | Allegiant Health | ANDA |
| 72288-756 | Famotidine 10 mg/1 Tablet, Film Coated | Amazon.com Services LLC | ANDA |
| 72288-470 | Cimetidine 200 mg/1 Tablet, Film Coated | Amazon.com Services LLC | ANDA |
| 58602-850 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Aurohealth LLC | ANDA |
| 58602-826 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Aurohealth LLC | ANDA |
| 58602-729 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Aurohealth LLC | ANDA |
| 63941-006 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Best Choice | ANDA |
| 37835-189 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Bi-Mart | ANDA |
| 70000-0521 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Cardinal Health | ANDA |
| 69842-659 | Famotidine 20 mg/1 Tablet, Film Coated | CVS Pharmacy | ANDA |
| 69842-679 | Esomeprazole Magnesium 20 mg/1 Tablet, Delayed Release | CVS Pharmacy | ANDA |
| 69842-941 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | CVS Pharmacy, Inc. | ANDA |
| 51316-511 | Famotidine 20 mg/1 Tablet, Film Coated | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | ANDA |
| 51316-816 | Famotidine 10 mg/1 Tablet, Film Coated | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | ANDA |
| 53943-016 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | DISCOUNT DRUG MART | ANDA |
| 43598-824 | Famotidine 10 mg/1 Tablet | Dr.Reddys Laboratories Inc. | ANDA |
| 43598-960 | Famotidine 20 mg/1 Tablet | Dr.Reddys Laboratories Inc. | ANDA |
| 55319-037 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Family Dollar Stores, LLC | ANDA |
| 55315-996 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Fred's, Inc. | ANDA |
| 85828-443 | Famotidine 20 mg/1 Tablet | Grocery Outlet | ANDA |
| 59640-023 | Famotidine 20 mg/1 Tablet, Film Coated | H E B | ANDA |
| 42507-194 | Famotidine 20 mg/1 Tablet, Film Coated | HyVee Inc | ANDA |
| 42507-141 | Famotidine 10 mg/1 Tablet, Film Coated | HyVee Inc | ANDA |
| 57483-120 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | INNOVUS PHARMACEUTICALS, INC. | ANDA |
| 30142-077 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | KROGER COMPANY | ANDA |
| 70000-0232 | Omeprazole Magnesium 20 mg/1 Capsule, Delayed Release | LEADER/ Cardinal Health 110, Inc. | ANDA |
| 80136-852 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | NORTHEAST PHARMA | ANDA |
| 56062-141 | Famotidine 10 mg/1 Tablet, Film Coated | Publix Super Markets Inc | ANDA |
| 56062-088 | Famotidine 20 mg/1 Tablet, Film Coated | Publix Super Markets Inc | ANDA |
| 69618-054 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | RELIABLE 1 LABORATORIES LLC | ANDA |
| 0536-1322 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Rugby Laboratories | ANDA |
| 49035-983 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Wal-Mart Stores, Inc. | ANDA |
| 0363-1008 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | WALGREEN CO. | ANDA |
| 0363-9977 | Esomeprazole Magnesium 20 mg/1 Tablet | Walgreens | ANDA |
| 67091-244 | Ranitidine Hydrochloride 75 mg/1 Tablet, Film Coated | WinCo Foods, LLC | ANDA |
| 67091-316 | Omeprazole Magnesium 20 mg/1 Tablet, Delayed Release | Winco Foods, LLC. | ANDA |
Acid Reducer recalls
- D-0026-2022 Oct 27, 2021 · Class II · Terminated
CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Frequently asked questions
What is Acid Reducer used for?
Uses • relieves heartburn associated with acid indigestion and sour stomach • prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages
Who makes Acid Reducer?
Acid Reducer is listed by 29 labelers in the FDA NDC directory, including 7-Eleven, Allegiant Health, Amazon.com Services LLC, Aurohealth LLC.
Has Acid Reducer been recalled?
The FDA enforcement database lists 1 recall for Acid Reducer, most recently D-0026-2022 (class ii): CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.