NDC 67751-202 Pepcid Complete
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67751 - Navajo Manufacturing Company Inc
- 67751-202 - Pepcid Complete
Product Characteristics
Product Packages
NDC Code 67751-202-01
Package Description: 1 POUCH in 1 CARTON / 1 TABLET, CHEWABLE in 1 POUCH
NDC Code 67751-202-02
Package Description: 2 POUCH in 1 CARTON / 1 TABLET, CHEWABLE in 1 POUCH
Product Details
What is NDC 67751-202?
What are the uses for Pepcid Complete?
Which are Pepcid Complete UNII Codes?
The UNII codes for the active ingredients in this product are:
- FAMOTIDINE (UNII: 5QZO15J2Z8)
- FAMOTIDINE (UNII: 5QZO15J2Z8) (Active Moiety)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- HYDROXIDE ION (UNII: 9159UV381P) (Active Moiety)
Which are Pepcid Complete Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- ACACIA (UNII: 5C5403N26O)
- HYDROXYPROPYL CELLULOSE (70000 WAMW) (UNII: 66O7AQV0RT)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- MINERAL OIL (UNII: T5L8T28FGP)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Pepcid Complete?
- RxCUI: 283641 - famotidine 10 MG / calcium carbonate 800 MG / magnesium hydroxide 165 MG Chewable Tablet
- RxCUI: 283641 - calcium carbonate 800 MG / famotidine 10 MG / magnesium hydroxide 165 MG Chewable Tablet
- RxCUI: 283641 - calcium carbonate 800 MG / famotidine 10 MG / milk of magnesia 165 MG Chewable Tablet
- RxCUI: 688892 - Pepcid Complete Dual Action 10 MG / 800 MG (Ca 320 MG) / 165 MG Chewable Tablet
- RxCUI: 688892 - calcium carbonate 800 MG / famotidine 10 MG / magnesium hydroxide 165 MG Chewable Tablet [Pepcid Complete]
* Please review the disclaimer below.
Patient Education
Calcium Carbonate
Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
[Learn More]
Famotidine
Prescription famotidine is used to treat ulcers (sores on the lining of the stomach or small intestine); gastroesophageal reflux disease (GERD, a condition in which backward flow of acid from the stomach causes heartburn and injury of the esophagus [tube that connects the mouth and stomach]); and conditions where the stomach produces too much acid, such as Zollinger-Ellison syndrome (tumors in the pancreas or small intestine that cause increased production of stomach acid). Over-the-counter famotidine is used to prevent and treat heartburn due to acid indigestion and sour stomach caused by eating or drinking certain foods or drinks. Famotidine is in a class of medications called H2 blockers. It works by decreasing the amount of acid made in the stomach.
[Learn More]
Magnesium Hydroxide
Magnesium hydroxide is used to treat occasional constipation in children and adults on a short-term basis. Magnesium hydroxide is in a class of medications called saline laxatives. It works by causing water to be retained with the stool. This increases the number of bowel movements and softens the stool so it is easier to pass.
[Learn More]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".