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  4. NDC Product Code: 55885-020 Roseday Rose

NDC 55885-020 Roseday Rose

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55885-020?
  4. Roseday Rose 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:
55885-020
Proprietary Name:
Roseday Rose
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lala Co., Ltd.
Labeler Code:
55885
Product Label ID:
2355413b-8127-42be-b45e-f72a1bd1dea5
Start Marketing Date: [9]
09-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 55885-020?

The NDC code 55885-020 is assigned by the FDA to the product Roseday Rose which is product labeled by Lala Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55885-020-02 1 container in 1 carton / 5 ml in 1 container (55885-020-01). 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 Roseday Rose?

Directions: This is a female secret care item and it is very effective to protect from infection and harmful diseases. Most of women can’t recognize the importance of secret zone. Rose Day Essential oil contains herb extracts and natural aroma oils so it can be used safely on the female secret zone. During usual day, Just drop a drop on the underwear. The natural extracts makes your pudenda more healthy and good smell will be maintained for a day.

Which are Roseday Rose UNII Codes?

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

Which are Roseday Rose 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".