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  4. NDC Product Code: 73587-0010 3seconds Magic Gargle Lemon

NDC 73587-0010 3seconds Magic Gargle Lemon

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73587-0010?
  5. 3seconds Magic Gargle Lemon Uses
  6. Active Ingredients UNII Codes
  7. 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:
73587-0010
Proprietary Name:
3seconds Magic Gargle Lemon
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sunjinbio Co.,ltd
Labeler Code:
73587
Product Label ID:
9e3071cd-0ae5-6b44-e053-2995a90a2d63
Start Marketing Date: [9]
01-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
14 MM
Imprint(s):
NONE
Score:
1
Flavor(s):
LEMON (C73396)

Product Packages

NDC Code 73587-0010-1

Package Description: 18 DOSE PACK in 1 BOX / 1 TABLET in 1 DOSE PACK

Product Details

What is NDC 73587-0010?

The NDC code 73587-0010 is assigned by the FDA to the product 3seconds Magic Gargle Lemon which is product labeled by Sunjinbio Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73587-0010-1 18 dose pack in 1 box / 1 tablet in 1 dose pack. 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 3seconds Magic Gargle Lemon?

1. Put one tablet in mouth.2. Chew it.3. Gargle for 30 sec.4. Spit it out.5. Rinse with water.

Which are 3seconds Magic Gargle Lemon UNII Codes?

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

Which are 3seconds Magic Gargle Lemon 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".