NDC 52642-225 Tropical Panned

NDC Product Code 52642-225

NDC CODE: 52642-225

Proprietary Name: Tropical Panned 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.

Non-Proprietary Name: 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.

Product Characteristics

Color(s):
YELLOW (C48330)
ORANGE (C48331)
PINK (C48328)
Shape: ROUND (C48348)
Size(s):
70 MM
Imprint(s):
AS
Flavor(s):
LEMON (C73396)
ORANGE (C73406)
STRAWBERRY (C73417)

NDC Code Structure

  • 52642 - Bestco Inc.

NDC 52642-225-32

Package Description: 32 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

Tropical Panned with NDC 52642-225 is a product labeled by Bestco Inc.. The generic name of Tropical Panned is . The product's dosage form is and is administered via form.

Labeler Name: Bestco Inc.

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.

  • CARNAUBA WAX (UNII: R12CBM0EIZ)

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: 03-19-2014 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".

* Please review the disclaimer below.

Information for Patients

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]
Simethicone

Simethicone is pronounced as (sye meth' i kone)
Why is simethicone medication prescribed?
Simethicone is used to treat the symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating.This medication is sometimes prescribed for other uses;...
[Read More]

* Please review the disclaimer below.

Tropical Panned Product Label Images

Tropical Panned 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 750 mgSimethicone 80 mg

Otc - Purpose

PurposeAntacidAnti-gas

Indications & Usage

  • Uses for the relief of:Acid indigestionHeartburnSour stomachUpset stomach associated with these symptomsBloating, pressure, or stuffed feeling commonl referred to as gas

Warnings

WarningsDo not use if you've 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 supervsion of a physician.Constipation may 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

  • DirectionsAdutls and children 12 years and older: Fully chew then swallow 1 or 2 chewable tablets are symptoms occur, or as directed by a doctor.Children under 12 years: consult a doctor.Do not take more than 5 chewable tablets in a 24 hour period.

Other Safety Information

  • Other informationeach chewable tablet contains: calcium 330 mgstore at room temperature. Avoid excessive heat above 40C (104F)Close cap tightly after use

Inactive Ingredient

Inactive ingredientsacacia, carmine, carnauba wax, citric acid, corn starch, corn syrup, FD&C Red #40 Aluminum Lake, flavors, hydrogenated coconut oil, hydrogenated vegetable oil, lecithin, maltodextrin, methyl paraben, modified starch, potassium hydroxide, pregelatinized modified starch, propyl paraben, propylene glycol, shellac, sorbic acid, sorbitol, sugar, titanium dioxide, triacetin, water, white wax

Otc - Questions

Questions1-800-986-0369

* Please review the disclaimer below.