NDC 81359-121 Flavobac Health Guard Complete

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:
81359-121
Proprietary Name:
Flavobac Health Guard Complete
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Oral Science Inc
Labeler Code:
81359
Start Marketing Date: [9]
05-14-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81359-121-11

Package Description: 1 BOTTLE in 1 BOX / 59 mL in 1 BOTTLE

Product Details

What is NDC 81359-121?

The NDC code 81359-121 is assigned by the FDA to the product Flavobac Health Guard Complete which is product labeled by Oral Science Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81359-121-11 1 bottle in 1 box / 59 ml in 1 bottle. 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 Flavobac Health Guard Complete?

Adults and children 2 years of age and older: apply 4 sprays to the affected area. Gargle, swish around, or allow to remain in place at least 1 minute and then spit out. Use up to 4 times daily or as directed by a dentist or doctorchildren under 12 years of age: should be supervised in the use of this product children under 2 years of age: not recommended

Which are Flavobac Health Guard Complete UNII Codes?

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

Which are Flavobac Health Guard Complete 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".