NDC 81744-010 S Gvd Phytoncide

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:
81744-010
Proprietary Name:
S Gvd Phytoncide
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Infinite Solution Co.
Labeler Code:
81744
Start Marketing Date: [9]
03-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81744-010-02

Package Description: 1 BOTTLE in 1 CARTON / 200 mL in 1 BOTTLE (81744-010-01)

NDC Code 81744-010-04

Package Description: 1 BOTTLE in 1 CARTON / 500 mL in 1 BOTTLE (81744-010-03)

Product Details

What is NDC 81744-010?

The NDC code 81744-010 is assigned by the FDA to the product S Gvd Phytoncide which is product labeled by Infinite Solution Co.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 81744-010-02 1 bottle in 1 carton / 200 ml in 1 bottle (81744-010-01), 81744-010-04 1 bottle in 1 carton / 500 ml in 1 bottle (81744-010-03). 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 S Gvd Phytoncide?

Use to refill this Phytoncide into Spray Apparatus

Which are S Gvd Phytoncide UNII Codes?

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

  • QUERCUS ACUTISSIMA WHOLE (UNII: 0TVP714IPW)
  • QUERCUS ACUTISSIMA WHOLE (UNII: 0TVP714IPW) (Active Moiety)
  • CHAMAECYPARIS OBTUSA WHOLE (UNII: 80ZNL1G5XY)
  • CHAMAECYPARIS OBTUSA WHOLE (UNII: 80ZNL1G5XY) (Active Moiety)
  • CRYPTOMERIA JAPONICA BARK (UNII: 5VB6Q5926T)
  • CRYPTOMERIA JAPONICA BARK (UNII: 5VB6Q5926T) (Active Moiety)

Which are S Gvd Phytoncide 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".