NDC 30142-557 Omeprazole
Tablet, Delayed Release Oral
Product Information
What is NDC 30142-557?
The NDC code 30142-557 is assigned by the FDA to the product Omeprazole which is a human over the counter drug product labeled by Kroger Company. The product's dosage form is tablet, delayed release and is administered via oral form. The product is distributed in 5 packages with assigned NDC codes 30142-557-01 1 bottle in 1 carton / 14 tablet, delayed release in 1 bottle, 30142-557-03 3 bottle in 1 carton / 14 tablet, delayed release in 1 bottle, 30142-557-30 2 carton in 1 carton / 14 blister pack in 1 carton / 1 tablet, delayed release in 1 blister pack, 30142-557-55 3 carton in 1 carton / 14 blister pack in 1 carton / 1 tablet, delayed release in 1 blister pack, 30142-557-74 14 blister pack in 1 carton / 1 tablet, delayed release in 1 blister pack. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.
What are the uses for Omeprazole?
Omeprazole is used to treat certain stomach and esophagus problems (such as acid reflux, ulcers). It works by decreasing the amount of acid your stomach makes. It relieves symptoms such as heartburn, difficulty swallowing, and persistent cough. This medication helps heal acid damage to the stomach and esophagus, helps prevent ulcers, and may help prevent cancer of the esophagus. Omeprazole belongs to a class of drugs known as proton pump inhibitors (PPIs). If you are self-treating with this medication, over-the-counter omeprazole products are used to treat frequent heartburn (occurring 2 or more days a week). Since it may take 1 to 4 days to have full effect, these products do not relieve heartburn right away. For over-the-counter products, carefully read the package instructions to make sure the product is right for you. Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar brand names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
Product Characteristics
Color(s) | BROWN (C48332) |
Shape | OVAL (C48345) |
Size(s) | 12 MM |
Imprint(s) | 20 |
Score | 1 |
Product Packages
NDC Code 30142-557-01
Package Description: 1 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 30142-557-03
Package Description: 3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 30142-557-30
Package Description: 2 CARTON in 1 CARTON / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
NDC Code 30142-557-55
Package Description: 3 CARTON in 1 CARTON / 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
NDC Code 30142-557-74
Package Description: 14 BLISTER PACK in 1 CARTON / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product Details
What are Omeprazole Active Ingredients?
- OMEPRAZOLE 20 mg/1 - A 4-methoxy-3,5-dimethylpyridyl, 5-methoxybenzimidazole derivative of timoprazole that is used in the therapy of STOMACH ULCERS and ZOLLINGER-ELLISON SYNDROME. The drug inhibits an H(+)-K(+)-EXCHANGING ATPASE which is found in GASTRIC PARIETAL CELLS.
Omeprazole Active Ingredients UNII Codes
- OMEPRAZOLE (UNII: KG60484QX9)
- OMEPRAZOLE (UNII: KG60484QX9) (Active Moiety)
NDC to RxNorm Crosswalk
- RxCUI: 402014 - omeprazole 20 MG Delayed Release Oral Tablet
- RxCUI: 402014 - omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral Tablet
Omeprazole Inactive Ingredients UNII Codes
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MONOETHANOLAMINE (UNII: 5KV86114PT)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
Pharmacologic Class(es)
* Please review the disclaimer below.
Patient Education
Omeprazole
Omeprazole is pronounced as (oh me' pray zol)
Why is omeprazole medication prescribed?
Prescription omeprazole is used alone or with other medications to treat gastroesophageal reflux disease (GERD), a condition in which backward flow of acid from the stoma...
[Read More]
* Please review the disclaimer below.
Omeprazole Product Label
FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Label Table of Contents
- ACTIVE INGREDIENT (IN EACH TABLET)
- PURPOSE
- USE
- WARNINGS
- DO NOT USE IF YOU HAVE:
- ASK A DOCTOR BEFORE USE IF YOU HAVE:
- ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE
- STOP USE AND ASK A DOCTOR IF:
- IF PREGNANT OR BREAST-FEEDING,
- KEEP OUT OF REACH OF CHILDREN.
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS OR COMMENTS?
- PRINCIPAL DISPLAY PANEL
Active Ingredient (In Each Tablet)
Omeprazole 20 mg
Purpose
Acid reducer
Use
• treats frequent heartburn (occurs 2 or more days a week)• not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect
Warnings
Allergy alert: Do not use if you are allergic to omeprazole
Do Not Use If You Have:
• trouble or pain swallowing food, vomiting with blood, or bloody or black stools• 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
These may be signs of a serious condition. See your doctor.
Ask A Doctor Before Use If You Have:
• had heartburn over 3 months. This may be a sign of a more serious condition.• frequent wheezing, particularly with heartburn• unexplained weight loss• nausea or vomiting• stomach pain
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• you need to take more than 1 course of treatment every 4 months• you get diarrhea• you develop a rash or joint pain
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).
Directions
• for adults 18 years of age and older• this product is to be used once a day (every 24 hours), every day for 14 days• it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours• swallow 1 tablet with a glass of water before eating in the morning• take every day for 14 days• do not take more than 1 tablet a day• do not use for more than 14 days unless directed by your doctor• swallow whole. Do not chew or crush tablets• you may repeat a 14-day course every 4 months• do not take for more than 14 days or more often than every 4 months unless directed by a doctor• children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition.
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
Other Information
• read the directions and warnings before use• keep the carton. It contains important information.• store at 20-25°C (68-77°F) and protect from moisture
Inactive Ingredients
carnauba wax, ferric oxide red, ferric oxide yellow, hypromellose, hypromellose acetate succinate, lactose monohydrate, monoethanolamine, propylene glycol, sodium lauryl sulfate, sodium starch glycolate, sodium stearate, sodium stearyl fumarate, talc, titanium dioxide, triethyl citrate
Questions Or Comments?
1-800-632-6900
Principal Display Panel
COMPARE TO PRILOSEC OTC®
OUR PHARMACIST RECOMMENDED
Omeprazole
Delayed Release Tablets 20 mg
ACID REDUCER
Treats FREQUENT Heartburn!
24 HR
actual size
42 TABLETS
Three14-Day Courses of Treatment
May Take 1 to 4 Days for Full Effect
* Please review the disclaimer below.