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  4. NDC Product Code: 49348-509 Sunmark Gas Relief

NDC 49348-509 Sunmark Gas Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49348-509?
  5. Sunmark Gas Relief Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
49348-509
Proprietary Name:
Sunmark Gas Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mckesson
Labeler Code:
49348
Product Label ID:
3fc6ab63-42cf-4fc6-8e98-d3fe1082ad62
Start Marketing Date: [9]
04-10-2004
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
14 MM
Imprint(s):
GDC156
Score:
1
Flavor(s):
PEPPERMINT (C73408)

Code Structure Chart

Product Details

What is NDC 49348-509?

The NDC code 49348-509 is assigned by the FDA to the product Sunmark Gas Relief which is product labeled by Mckesson. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49348-509-07 3 blister pack in 1 carton / 12 tablet, chewable in 1 blister pack. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sunmark Gas Relief?

Chew 1 to 2 tablets thoroughly as needed after meals and at bedtimedo not exceed 6 tablets per day unless directed by a physician.Other informationdo not use if any individual blister unit is broken or open.store at room temperature.avoid high humidity and excessive heat, above 40°C (104°F)

Which are Sunmark Gas Relief UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sunmark Gas Relief 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:

What is the NDC to RxNorm Crosswalk for Sunmark Gas Relief?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

* Please review the disclaimer below.

Patient Education

Simethicone


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; ask your doctor or pharmacist for more information.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

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

[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".