NDC 49726-025 Thyroveev Hyperthyroid Symptom Relief

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:
49726-025
Proprietary Name:
Thyroveev Hyperthyroid Symptom Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hello Life, Inc.
Labeler Code:
49726
Start Marketing Date: [9]
08-15-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49726-025-02

Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 59 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 49726-025?

The NDC code 49726-025 is assigned by the FDA to the product Thyroveev Hyperthyroid Symptom Relief which is product labeled by Hello Life, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49726-025-02 1 bottle, dropper in 1 carton / 59 ml in 1 bottle, dropper. 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 Thyroveev Hyperthyroid Symptom Relief?

Dispense Thyroveev directly into mounth, or add recommended dosage into 8-12 oz purified (non-chlorinated) water and drink. Safe for ages 2 and up. DOSAGE BY WEIGHT30-50 lbs (13.6-22.6 kg) 1/2 mL twice per day50+ lbs (22.6+ kg) 1 mL twice per day

Which are Thyroveev Hyperthyroid Symptom Relief UNII Codes?

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

Which are Thyroveev Hyperthyroid Symptom Relief 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".