NDC 61722-260 Flormar Perfect Coverage Foundation 115 Toffee

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:
61722-260
Proprietary Name:
Flormar Perfect Coverage Foundation 115 Toffee
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kosan Kozmetik Sanayi Ve Ticaret A.s.
Labeler Code:
61722
Start Marketing Date: [9]
09-27-2015
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61722-260-00

Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE

Product Details

What is NDC 61722-260?

The NDC code 61722-260 is assigned by the FDA to the product Flormar Perfect Coverage Foundation 115 Toffee which is product labeled by Kosan Kozmetik Sanayi Ve Ticaret A.s.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61722-260-00 1 bottle in 1 box / 30 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 Flormar Perfect Coverage Foundation 115 Toffee?

Shake well before use.Apply liberally 15 minutes before sun exposure.Reapply at least every 2 hours.Use a water resistant sunscreen if swimming or sweating.Sun Protection Measures.  Spending time in the sun increases cancer and early skin aging.  To decrease this risk, regularly use a Broad Spectrum SPF value of15 or higher and other sun protection measures including:Limit timein the sun, especially from 10 a.m. - 2 p.m.Wear long-sleeved shirts, pants, hats and sunglasses.Children under 6 months of age:  Ask a doctor.

Which are Flormar Perfect Coverage Foundation 115 Toffee UNII Codes?

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

Which are Flormar Perfect Coverage Foundation 115 Toffee 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:

* Please review the disclaimer below.

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".