NDC 24202-002 Calcid Antacid Calcium Supplement Regular Strength

  1. Labeler Index
  2. Pro-ventas S.a. De C.v.
  3. NDC: 24202-002 Calcid Antacid Calcium Supplement Regular Strength

NDC Product Code 24202-002

NDC CODE: 24202-002

Proprietary Name: Calcid Antacid Calcium Supplement Regular Strength What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as purposeantacid

Product Characteristics

Color(s):
ORANGE (C48331 - ORANGE, YELLOW, RED)
Shape: ROUND (C48348)
Size(s):
16 MM
Imprint(s):
CALCID
Score: 1
Flavor(s):
FRUIT (C73389 - MIXED FRUIT)

NDC Code Structure

NDC 24202-002-10

Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Calcid Antacid Calcium Supplement Regular Strength with NDC 24202-002 is product labeled by Pro-ventas S.a. De C.v.. The product's dosage form is and is administered via form.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates multiple concept unique identifiers (RXCUI) are associated with this product:


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • SUCROSE (UNII: C151H8M554)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • TALC (UNII: 7SEV7J4R1U)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • CALCIUM STEARATE (UNII: 776XM7047L)
  • ADIPIC ACID (UNII: 76A0JE0FKJ)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • D&C RED NO. 6 (UNII: 481744AI4O)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • D&C RED NO. 27 (UNII: 2LRS185U6K)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Pro-ventas S.a. De C.v.
Labeler Code: 24202
Start Marketing Date: 12-30-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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Information for Patients



is


...
[Read More]
Calcium Carbonate

Calcium Carbonate is pronounced as (kal' see um) (kar' bon ate)
Why is calcium carbonate medication prescribed?
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, nervo...
[Read More]

* Please review the disclaimer below.

Calcid Antacid Calcium Supplement Regular Strength Product Label Images

Calcid Antacid Calcium Supplement Regular Strength Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredient (per tablet)Calcium carbonate USP 500 mg

Otc - Purpose

PurposeAntacid

Indications & Usage

Uses relieves: heartburn, sour stomach, acid indigestion, upset stomach associated with these symptoms

Warnings

WarningsAsk a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs

Otc - When Using

When using this product-do not take more than 15 tablets in 24 hours-do not use the maximum dosage for more than 2 weeks

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Dosage & Administration

Directions Antacid-chew 2-4 tablets as symptoms occur or as directed by a doctor

Other

Other information- for calcium content see Supplement Facts.- Store below30°C (86°F)- do not use if printed seal under cap is torn or missingCALCIUM SUPPLEMENTUses: As a daily source of extra calciumDirections: chew 2 tablets twice daily with mealSupplement FactsServing Size: 2 TabletsServings Per Container: 50Amount              %DailyPer Serving         ValueCalories 5Sugars 1gCalcium 400mg     40%

Inactive Ingredient

Inactive Ingredientssucrose, calcium carbonate, corn starch, talc, mineral oil, calcium sterate, natural flavor and artificial flavor, adpic acid, Yellow No. 5, Yellow No. 6, Red No. 6, Red No. 30, Red No. 27 and Blue No. 1

Otc - Questions

Questions? 1-877 2198302

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