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  4. NDC Product Code: 55910-850 Womens Gentle Laxative

NDC 55910-850 Womens Gentle Laxative

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55910-850?
  5. Womens Gentle Laxative Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55910-850
Proprietary Name:
Womens Gentle Laxative
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dolgencorp, Inc.
Labeler Code:
55910
Product Label ID:
7c510c71-db3f-4351-88ad-ddc9929e7a48
Start Marketing Date: [9]
05-14-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
F
Score:
1

Product Packages

NDC Code 55910-850-25

Package Description: 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK

Product Details

What is NDC 55910-850?

The NDC code 55910-850 is assigned by the FDA to the product Womens Gentle Laxative which is product labeled by Dolgencorp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55910-850-25 25 tablet, delayed release 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 Womens Gentle Laxative?

Take with a glass of wateradults and children 12 years and over1 to 3 tablets in a single daily dosechildren 6 to under 12 years of age1 tablet in a single daily dosechildren under 6 years of ageask a doctor

Which are Womens Gentle Laxative UNII Codes?

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

Which are Womens Gentle Laxative 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:

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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".