NDC 0135-0606 Tums Chewy Bites

NDC Product Code 0135-0606

NDC CODE: 0135-0606

Proprietary Name: Tums Chewy Bites 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

Color(s):
RED (C48326 - RED, PINK, PURPLE)
Shape: ROUND (C48348)
Size(s):
19 MM
Imprint(s):
T
Score: 1
Flavor(s):
STRAWBERRY (C73417 - ASSORTED BERRY: STRAWBERRY, RASPBERRY, MIXED BERRY)

NDC Code Structure

NDC 0135-0606-01

Package Description: 32 TABLET, CHEWABLE in 1 BOTTLE

Price per Unit: $0.06442 per EA

NDC 0135-0606-02

Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE

Price per Unit: $0.06442 per EA

NDC 0135-0606-04

Package Description: 8 TABLET, CHEWABLE in 1 BOTTLE

NDC 0135-0606-05

Package Description: 2 BOTTLE in 1 PACKAGE > 54 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

Tums Chewy Bites with NDC 0135-0606 is a product labeled by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1044532 and 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.

  • ACACIA (UNII: 5C5403N26O)
  • ALCOHOL (UNII: 3K9958V90M)
  • AMMONIA (UNII: 5138Q19F1X)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • CARMINIC ACID (UNII: CID8Z8N95N)
  • CARNAUBA WAX (UNII: R12CBM0EIZ)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • CORN SYRUP (UNII: 9G5L16BK6N)
  • ICODEXTRIN (UNII: 2NX48Z0A9G)
  • ETHYL ACETATE (UNII: 76845O8NMZ)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • MALTODEXTRIN (UNII: 7CVR7L4A2D)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)
  • BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
  • PHOSPHORIC ACID (UNII: E4GA8884NN)
  • POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • SHELLAC (UNII: 46N107B71O)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • SORBIC ACID (UNII: X045WJ989B)
  • SORBITOL (UNII: 506T60A25R)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
  • SUCROSE (UNII: C151H8M554)
  • TERT-BUTYLHYDROQUINONE (UNII: C12674942B)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • TRIACETIN (UNII: XHX3C3X673)

Product Labeler Information

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

Labeler Name: Glaxosmithkline Consumer Healthcare Holdings (us) Llc
Labeler Code: 0135
Start Marketing Date: 03-01-2017 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: 12-31-2022 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

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...
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is

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Tums Chewy Bites Product Label Images

Tums Chewy Bites 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

Active Ingredient (Per Tablet)

Calcium Carbonate USP 750mg

Purpose

Antacid

Uses

  • Relieves •heartburn •acid indigestion •sour stomach •upset stomach associated with these symptoms

Ask A Doctor Or Pharmacist Before Use If You Are

Presently taking a prescription drug. Antacids may interact with certain prescription drugs.

When Using This Product

  • •do not take more than 6 tablets in 24 hours •if pregnant do not take more than 6 tablets in 24 hours •do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

Directions

  • •adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor •do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other Information

  • •each chewable tablet contains: elemental calcium 300mg •do not store above 25°C (77°F)

Inactive Ingredients

Acacia gum, alcohol, ammonium hydroxide, beeswax, caprylic/capric triglycerides, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, ethyl alcohol, FD&C blue #1 alum lake, FD&C blue #2 alum lake, FD&C red #40, FD&C red #40 alum lake, FD&C yellow #5 alum lake (tartrazine), FD&C yellow #6, FD&C yellow #6 alum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methyl paraben, modified corn starch, n-butyl alcohol, phosphoric acid, PVP, propyl paraben, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy bean oil, soy lecithin, sucrose, TBHQ, titanium dioxide, triacetin, vegetable oil

Questions?

Call 1-800-897-7535

* Please review the disclaimer below.