NDC 74955-035 Breeze Sanitizing Citrus Fresh Scent

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:
74955-035
Proprietary Name:
Breeze Sanitizing Citrus Fresh Scent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
74955
Start Marketing Date: [9]
09-05-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 74955-035?

The NDC code 74955-035 is assigned by the FDA to the product Breeze Sanitizing Citrus Fresh Scent which is product labeled by Cosmolive Kozmetik Sanayi Ve Ticaret Anonim Sirketi. The product's dosage form is . The product is distributed in a single package with assigned NDC code 74955-035-01 550 ml in 1 bottle, spray . 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 Breeze Sanitizing Citrus Fresh Scent?

• Shake well before use.• Hold can upright at 6-7 Inches away from surfaces and spray evenly.• Allow to air dry for 5 to 10 minutes. Repeat application a necessary• Supervise children under 6 years of age when using this product to avoid swallowing

Which are Breeze Sanitizing Citrus Fresh Scent UNII Codes?

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

Which are Breeze Sanitizing Citrus Fresh Scent 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:

What is the NDC to RxNorm Crosswalk for Breeze Sanitizing Citrus Fresh Scent?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".