NDC 15127-549 Laxative Pills

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
15127-549
Proprietary Name:
Laxative Pills
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
15127
Start Marketing Date: [9]
12-12-2008
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
G177
Score:
1

Code Structure Chart

Product Details

What is NDC 15127-549?

The NDC code 15127-549 is assigned by the FDA to the product Laxative Pills which is product labeled by Select Brand. The product's dosage form is . The product is distributed in a single package with assigned NDC code 15127-549-24 2 blister pack in 1 package / 12 pill 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 Laxative Pills?

Swallow tablets(s) with a glass of waterswallow tablets(s) whole, do not crush, break or chew adults and children 12 years and over take 2 tablets once or twice daily with a glass of water children 6 to under 12 years take 1 tablet once or twice daily with a glass of water children under 6 years ask a doctor

Which are Laxative Pills UNII Codes?

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

Which are Laxative Pills 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 Laxative Pills?

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 indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".