NDC 37808-353 Heb Gentle Laxative

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:
37808-353
Proprietary Name:
Heb Gentle Laxative
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H E B
Labeler Code:
37808
Start Marketing Date: [9]
02-13-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
BULLET (C48335)
Size(s):
34 MM

Product Packages

NDC Code 37808-353-08

Package Description: 2 BLISTER PACK in 1 CARTON / 40 mg in 1 BLISTER PACK

Product Details

What is NDC 37808-353?

The NDC code 37808-353 is assigned by the FDA to the product Heb Gentle Laxative which is product labeled by H E B. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37808-353-08 2 blister pack in 1 carton / 40 mg 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 Heb Gentle Laxative?

Adults and children 12 years of age and older                           Children 6 to under 12 years                     Children under 6One suppository once daily                                                        1/2 suppository once daily                        Ask doctor.-Detach one suppository from the strip and remove from foil - Carefully insert one suppositry well into the rectum-Do not use more than once per day

Which are Heb Gentle Laxative UNII Codes?

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

Which are Heb 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:

What is the NDC to RxNorm Crosswalk for Heb Gentle Laxative?

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:

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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".