NDC 63868-035 Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint
Calcium Carbonate Tablet, Chewable Oral - View Dosage, Usage, Ingredients, Routes, UNII
- Product Information
- Product Packages
- Product Characteristics
- What is NDC 63868-035?
- Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint Uses
- Active Ingredients
- Active Ingredients UNII Codes
- Inactive Ingredients UNII Codes
- NDC to RxNorm Crosswalk
- Pharmacologic Classes
- Patient Education
Product Information
- 63868 - Chain Drug Marketing Association Inc.
- 63868-035 - Quality Choice Regular Strength Antacid Peppermint
Product Characteristics
Product Packages
NDC Code 63868-035-15
Package Description: 150 TABLET, CHEWABLE in 1 BOTTLE
Product Details
What is NDC 63868-035?
What are the uses for Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint?
What are Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint Active Ingredients?
- CALCIUM CARBONATE 500 mg/1 - Carbonic acid calcium salt (CaCO3). An odorless, tasteless powder or crystal that occurs in nature. It is used therapeutically as a phosphate buffer in hemodialysis patients and as a calcium supplement.
Which are Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
Which are Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- CROSPOVIDONE (UNII: 68401960MK)
What is the NDC to RxNorm Crosswalk for Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint?
- RxCUI: 308907 - calcium carbonate 500 MG (Ca 200 MG) Chewable Tablet
- RxCUI: 308907 - calcium carbonate 500 MG Chewable Tablet
- RxCUI: 308907 - calcium carbonate 500 MG (equivalent to calcium 200 MG) Chewable Tablet
Which are the Pharmacologic Classes for Quality Choice Regular Strength Antacid Peppermint Regular Strength Antacid Peppermint?
* 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.
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* Please review the disclaimer below.
[1] 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.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] 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.
[8] 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.
[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".