NDC 73298-190 Wedol Water-based Personal Lubricant

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:
73298-190
Proprietary Name:
Wedol Water-based Personal Lubricant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhenshi Huaxiang Technology Co.,ltd.
Labeler Code:
73298
Start Marketing Date: [9]
09-15-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 73298-190-34

Package Description: 1 TUBE in 1 BOX / 240 mL in 1 TUBE (73298-190-33)

Product Details

What is NDC 73298-190?

The NDC code 73298-190 is assigned by the FDA to the product Wedol Water-based Personal Lubricant which is product labeled by Shenzhenshi Huaxiang Technology Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73298-190-34 1 tube in 1 box / 240 ml in 1 tube (73298-190-33). 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 Wedol Water-based Personal Lubricant?

This product is used as

Which are Wedol Water-based Personal Lubricant UNII Codes?

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

  • HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5)
  • HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5) (Active Moiety)

Which are Wedol Water-based Personal Lubricant 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".