NDC 76168-501 Allergy Relief 24hr

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:
76168-501
Proprietary Name:
Allergy Relief 24hr
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Velocity Pharma Llc
Labeler Code:
76168
Start Marketing Date: [9]
07-02-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
8 MM
Imprint(s):
X;X
Score:
2

Product Packages

NDC Code 76168-501-10

Package Description: 1 BOTTLE in 1 CARTON / 10 TABLET in 1 BOTTLE

NDC Code 76168-501-11

Package Description: 1 BOTTLE in 1 CARTON / 100 TABLET in 1 BOTTLE

NDC Code 76168-501-18

Package Description: 1 BOTTLE in 1 CARTON / 180 TABLET in 1 BOTTLE

NDC Code 76168-501-24

Package Description: 1 BOTTLE in 1 CARTON / 240 TABLET in 1 BOTTLE

Product Details

What is NDC 76168-501?

The NDC code 76168-501 is assigned by the FDA to the product Allergy Relief 24hr which is product labeled by Velocity Pharma Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 76168-501-10 1 bottle in 1 carton / 10 tablet in 1 bottle, 76168-501-11 1 bottle in 1 carton / 100 tablet in 1 bottle, 76168-501-18 1 bottle in 1 carton / 180 tablet in 1 bottle, 76168-501-24 1 bottle in 1 carton / 240 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 Allergy Relief 24hr?

Adults 65 years of age and older■ ask a doctoradults and children 12-64 years of age ■ take 1 tablet (5 mg) once daily in the evening ■ do not take more than 1 tablet (5 mg) in 24 hours ■ ½ tablet (2.5 mg) once daily in the evening may be appropriate for less severe symptoms children 6-11 years of age■ take ½ tablet (2.5 mg) once daily in the evening ■ do not take more than ½ tablet (2.5 mg) in 24 hours children under 6 years of age■ do not useconsumers with kidney disease■ do not use(Note: Age ranges are bolded in the draft container labeling for tablet bottle)

Which are Allergy Relief 24hr UNII Codes?

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

  • LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA)
  • LEVOCETIRIZINE (UNII: 6U5EA9RT2O) (Active Moiety)

Which are Allergy Relief 24hr 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 Allergy Relief 24hr?

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:
  • RxCUI: 855172 - levocetirizine dihydrochloride 5 MG Oral Tablet
  • RxCUI: 855172 - levocetirizine dihydrochloride 5 MG 24 HR Oral Tablet

* Please review the disclaimer below.

Patient Education

Levocetirizine


Levocetirizine is used to relieve runny nose; sneezing; and redness, itching, and tearing of the eyes caused by hay fever, seasonal allergies, and allergies to other substances such as dust mites, animal dander, and mold. It is also used to treat symptoms of hives, including itching and rash. Levocetirizine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
[Learn More]


* 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".