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  4. NDC Product Code: 69697-993 Kimvent Oral Care Suction Swab Pack

NDC 69697-993 Kimvent Oral Care Suction Swab Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69697-993?
  5. Kimvent Oral Care Suction Swab Pack 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:
69697-993
Proprietary Name:
Kimvent Oral Care Suction Swab Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Halyard Health
Labeler Code:
69697
Product Label ID:
b1325ab5-6667-4f22-a625-8e91fe543c11
Start Marketing Date: [9]
08-26-2008
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
MINT (C73404)

Code Structure Chart

Product Details

What is NDC 69697-993?

The NDC code 69697-993 is assigned by the FDA to the product Kimvent Oral Care Suction Swab Pack which is product labeled by Halyard Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69697-993-01 1 kit in 1 carton * 14 ml in 1 cup * 2 g in 1 tube. 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 Kimvent Oral Care Suction Swab Pack?

Topical dosage for adults and children 3 years of age and older is a rinse used no more than 4 times daily. For children under 3 years of age, there is no recommended dosage except under the advice and supervision of a dentist or doctor.Use only under health care practitioners supervision.

Which are Kimvent Oral Care Suction Swab Pack UNII Codes?

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

Which are Kimvent Oral Care Suction Swab Pack 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".