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  4. NDC Product Code: 81762-101 Evitarol

NDC 81762-101 Evitarol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81762-101?
  4. Evitarol Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
81762-101
Proprietary Name:
Evitarol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Maierto Inc
Labeler Code:
81762
Product Label ID:
be3b65c3-8909-0917-e053-2995a90a7bcd
Start Marketing Date: [9]
04-26-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81762-101-50

Package Description: 1 BOTTLE, PUMP in 1 BOX / 50 [hp_C] in 1 BOTTLE, PUMP

Product Details

What is NDC 81762-101?

The NDC code 81762-101 is assigned by the FDA to the product Evitarol which is product labeled by Maierto Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81762-101-50 1 bottle, pump in 1 box / 50 [hp_c] in 1 bottle, pump. 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 Evitarol?

Uses*Temporarily relieves upper respiratory, COVID like symptoms. *THESE “USES” HAVE NOT BEEN EVALUATED BY THE FOOD AND DRUG ADMINISTRATION.

Which are Evitarol UNII Codes?

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

  • BOVINE TUBERCULIN (UNII: HKD62G79N5)
  • BOVINE TUBERCULIN (UNII: HKD62G79N5) (Active Moiety)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
  • CRYPTOLEPIS SANGUINOLENTA WHOLE (UNII: 9Q3JWJ3GXG)
  • CRYPTOLEPIS SANGUINOLENTA WHOLE (UNII: 9Q3JWJ3GXG) (Active Moiety)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)
  • INFLUENZA A VIRUS A/HONG KONG/2671/2019 (H3N2) NIB-121 NEURAMINIDASE ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: 2828WNW8HO)
  • INFLUENZA A VIRUS A/HONG KONG/2671/2019 (H3N2) NIB-121 NEURAMINIDASE ANTIGEN (UV, FORMALDEHYDE INACTIVATED) (UNII: 2828WNW8HO) (Active Moiety)
  • INFLUENZA B VIRUS B/WASHINGTON/02/2019 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: VEH9U90EHX)
  • INFLUENZA B VIRUS B/WASHINGTON/02/2019 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: VEH9U90EHX) (Active Moiety)
  • SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
  • SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • INFLUENZA A VIRUS A/GUANGDONG-MAONAN/SWL1536/2019 CNIC-1909 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: NY1FF92M1E)
  • INFLUENZA A VIRUS A/GUANGDONG-MAONAN/SWL1536/2019 CNIC-1909 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: NY1FF92M1E) (Active Moiety)
  • RANCID BEEF (UNII: 29SUH5R3HU)
  • RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
  • INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: B93BQX9789)
  • INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: B93BQX9789) (Active Moiety)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
  • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)

Which are Evitarol 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:

* 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".