NDC 52642-227 Assorted Fruit

NDC Product Code 52642-227

NDC CODE: 52642-227

Proprietary Name: Assorted Fruit 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.

Product Characteristics

ORANGE (C48331)
YELLOW (C48330)
PINK (C48328)
Shape: ROUND (C48348)
70 MM
LEMON (C73396)
ORANGE (C73406)

NDC Code Structure

  • 52642 - Bestco Inc

NDC 52642-227-36

Package Description: 36 TABLET, CHEWABLE in 1 BOTTLE

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

NDC Product Information

Assorted Fruit with NDC 52642-227 is a product labeled by Bestco Inc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 308915.

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.


Product Labeler Information

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

Labeler Name: Bestco Inc
Labeler Code: 52642
Start Marketing Date: 08-31-2015 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: 12-31-2019 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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Assorted Fruit Product Label Images

Assorted Fruit 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

Calcium Carbonate 750mg

Otc - Purpose


Indications & Usage

  • Uses for the relief of:
  • Acid indigestionheartburnsour stomachupset stomach associated with these symptoms


WarningsDo not use if you have ever had an allergic reaction to this product or any of its ingredients

Otc - Ask Doctor/Pharmacist

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

Otc - When Using

  • When using this productdo not take more than 5 chewable tablets in a 24 hour perioddo not use the maximum dosage of this product for more than 2 weeks except under the advice and supervision of a physicianconstipation my occur

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Dosage & Administration

  • Directionsadults and children 12 years and over: fully chew then swallow 1 or 2 chewable tablets as symptoms occur, or as directed by a doctorchildren under 12 years : consult a doctordo not take more than 5 hcewable talbets in a 24-hour period

Other Safety Information

  • Other informationeach chewable tablet contains: calcium 300 mgcontains FD&C Yellow No.5 (tartazine) as a color additivestore at room temperature. Avoid humidity.close cap tightly after use

Inactive Ingredient

Inactive Ingredientsacacia, carmine, carnumba wax, citric acid, corn starch, DL-alpha tocopherol, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #5 aluminum lake (tartazine), FD&C yellow #6, FD&C yellow #6 aluminum lake, FD&C yellow #6 lake, flavors, hydrogenated coconut oil, hydrogenated vegetable oil, lecithin, medium chain triglycerides, methyl paraben, modified starch, phosphoric acid, pregelatinized modified starch, propyl paraben, propylene glycol, shellac, sodium benzoate, sorbic acid, sorbitol, sugar, titanium dioxide, water, white wax

Otc - Questions


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