NDC 11822-0850 Childrens Loratadine

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:
11822-0850
Proprietary Name:
Childrens Loratadine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid Corporation
Labeler Code:
11822
Start Marketing Date: [9]
08-20-2004
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - COLORLESS TO SLIGHTLY YELLOW)
Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 11822-0850-8

Package Description: 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE

Product Details

What is NDC 11822-0850?

The NDC code 11822-0850 is assigned by the FDA to the product Childrens Loratadine which is product labeled by Rite Aid Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-0850-8 1 bottle in 1 carton / 120 ml 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 Childrens Loratadine?

Adults and children 6 years and over2 teaspoonfuls daily; do not take more than 2 teaspoonfuls in 24 hourschildren 2 to under 6 years of age1 teaspoonful daily; do not take more than 1 teaspoonful in 24 hoursconsumers with liver or kidney diseaseask a doctor

Which are Childrens Loratadine UNII Codes?

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

Which are Childrens Loratadine 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 Childrens Loratadine?

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".