NDC 75360-1145 Immunitea Herbal Relief Tea

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:
75360-1145
Proprietary Name:
Immunitea Herbal Relief Tea
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hemani International
Labeler Code:
75360
Start Marketing Date: [9]
07-22-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75360-1145-1

Package Description: 28 g in 1 BOX, UNIT-DOSE

Product Details

What is NDC 75360-1145?

The NDC code 75360-1145 is assigned by the FDA to the product Immunitea Herbal Relief Tea which is product labeled by Hemani International. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75360-1145-1 28 g in 1 box, unit-dose . 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 Immunitea Herbal Relief Tea?

Take 1 1/2 cup of water. Add 1 Tea Bag. Boil the water along with the tea bag for 10 minutes. Pour the water into a cup and conume the warm tea. Sweeten with honey if desired.ADULT: Drink 2 times a day, after a meal.CHILD (11-15 years): Drink 1 cup a day, after a mealDuration of Use: 7 days

Which are Immunitea Herbal Relief Tea UNII Codes?

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

Which are Immunitea Herbal Relief Tea 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".