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  4. NDC Product Code: 69720-4001 Singiso 102 (0.8g)

NDC 69720-4001 Singiso 102 (0.8g)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69720-4001?
  5. Singiso 102 (0.8g) 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:
69720-4001
Proprietary Name:
Singiso 102 (0.8g)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sae In Dang Co., Ltd.
Labeler Code:
69720
Product Label ID:
3b7fdf98-f3b4-1273-e054-00144ff88e88
Start Marketing Date: [9]
08-31-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)
Shape:
OVAL (C48345)
Size(s):
180 MM
Score:
2

Product Packages

NDC Code 69720-4001-1

Package Description: 30 g in 1 BOX

Product Details

What is NDC 69720-4001?

The NDC code 69720-4001 is assigned by the FDA to the product Singiso 102 (0.8g) which is product labeled by Sae In Dang Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69720-4001-1 30 g in 1 box . 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 Singiso 102 (0.8g)?

This product is used as Stimulant. To help the treatment and prevention of blood circulation, antioxidant effect, memory improvement, prostate, erectile dysfunction

Which are Singiso 102 (0.8g) UNII Codes?

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

Which are Singiso 102 (0.8g) 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".