NDC 73298-190 Wedol Water-based Personal Lubricant

Water-based Personal Lubricant

NDC Product Code 73298-190

NDC Code: 73298-190

Proprietary Name: Wedol Water-based Personal Lubricant What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Water-based Personal Lubricant What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 73298 - Shenzhenshi Huaxiang Technology Co.,ltd.
    • 73298-190 - Wedol Water-based Personal Lubricant

NDC 73298-190-34

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

NDC Product Information

Wedol Water-based Personal Lubricant with NDC 73298-190 is a a human over the counter drug product labeled by Shenzhenshi Huaxiang Technology Co.,ltd.. The generic name of Wedol Water-based Personal Lubricant is water-based personal lubricant. The product's dosage form is oil and is administered via topical form.

Labeler Name: Shenzhenshi Huaxiang Technology Co.,ltd.

Dosage Form: Oil - An unctuous, combustible substance which is liquid, or easily liquefiable, on warming, and is soluble in ether but insoluble in water. Such substances, depending on their origin, are classified as animal, mineral, or vegetable oils.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Wedol Water-based Personal Lubricant Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYDROXYETHYL CELLULOSE (140 CPS AT 5%) 3.84 g/240mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • PEG-7 DISTEARATE (UNII: VU1ZWG290C)
  • WATER (UNII: 059QF0KO0R)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Shenzhenshi Huaxiang Technology Co.,ltd.
Labeler Code: 73298
Marketing Category: UNAPPROVED DRUG OTHER - 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.

Start Marketing Date: 09-15-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

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