NDC 55319-351 Regular Strength Acid Reducer

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:
55319-351
Proprietary Name:
Regular Strength Acid Reducer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Family Dollar
Labeler Code:
55319
Start Marketing Date: [9]
06-28-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
OVAL (C48345)
Size(s):
12 MM
Imprint(s):
9R
Score:
1

Product Packages

NDC Code 55319-351-24

Package Description: 3 BLISTER PACK in 1 CARTON / 8 TABLET in 1 BLISTER PACK

NDC Code 55319-351-65

Package Description: 1 BOTTLE in 1 CARTON / 65 TABLET in 1 BOTTLE

Product Details

What is NDC 55319-351?

The NDC code 55319-351 is assigned by the FDA to the product Regular Strength Acid Reducer which is product labeled by Family Dollar. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 55319-351-24 3 blister pack in 1 carton / 8 tablet in 1 blister pack, 55319-351-65 1 bottle in 1 carton / 65 tablet in 1 bottle. 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 Regular Strength Acid Reducer?

•adults and children 12 years and over:•to relieve symptoms, swallow 1 tablet with a glass of water•to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutesbefore eating food or drinking beverages that cause heartburn•can be used up to twice daily (do not take more than 2 tablets in 24 hours)•children under 12 years: ask a doctor 

Which are Regular Strength Acid Reducer UNII Codes?

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

Which are Regular Strength Acid Reducer 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 Regular Strength Acid Reducer?

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:

* 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".