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  4. NDC Product Code: 55618-2006 Secret Gyno (10 Tablets)

NDC 55618-2006 Secret Gyno (10 Tablets)

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55618-2006?
  5. Secret Gyno (10 Tablets) 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.

Get all the details for National Drug Code (NDC) 55618-2006 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
55618-2006
Proprietary Name:
Secret Gyno (10 Tablets)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Haudongchun Co., Ltd.
Labeler Code:
55618
Product Label ID:
3e5e00bd-2c32-41d6-b409-24cc94abb8c4
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
03-15-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
14 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 55618-2006?

The NDC code 55618-2006 is assigned by the FDA to the product Secret Gyno (10 Tablets) which is product labeled by Haudongchun Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55618-2006-3 1 blister pack in 1 package / 10 capsule in 1 blister pack (55618-2006-2) / 600 mg in 1 capsule (55618-2006-1). 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 Secret Gyno (10 Tablets)?

For adults – 2 tablets at the same time- Keep use 2 days consecutively and prefer to use once 10 days in 2 months. (after then, use it when you need)- Do not use up to 6 hours prior to any sexual relation.- Do not use up to 6 months after giving birth.- Symptoms may vary depending on the age of the patient.Directions- Use only adults and children 12 years age and over1) Wash hands before using this product2) Do not remove moisture, open the package and vaginal tablets are placed into the vagina in much the same way as a tampon stand, squat, or lie on your back in a comfortable position then insert the loaded applicator into the vagina as far as it will comfortably go.3) It is preferable to use the treatment during night time prior to bed.4) Use of a sanitary pad after application, because there may be vaginal secretion 30min after application. If there are lots of secretion, change a new sanitary pad.5) Wash the area around the vagina (the vulva) gently next day, bacteria in your vaginal secretion can cause itching.

Which are Secret Gyno (10 Tablets) UNII Codes?

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

Which are Secret Gyno (10 Tablets) 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".