NDC 70592-030 Freeze 24 7 Anti Gravity Lifting Face Mask

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:
70592-030
Proprietary Name:
Freeze 24 7 Anti Gravity Lifting Face Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
70592
Start Marketing Date: [9]
03-02-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70592-030?

The NDC code 70592-030 is assigned by the FDA to the product Freeze 24 7 Anti Gravity Lifting Face Mask which is product labeled by Summit C&t Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70592-030-02 1 cello pack in 1 carton / 30 ml in 1 cello pack (70592-030-01). 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 Freeze 24 7 Anti Gravity Lifting Face Mask?

How to use: 1. Remove mask from the sachet and gently unfold. 2. Peel off the protective paper from one side of the mask. 3. Apply the mask to cleansed and dry face, fitting it to the curves around the eyes, nose and mouth. 4. Once fully applied to face, remove the protective film from the outside of the mask. 5. Leave on for 20-25 minutes then discard. 6. Gently pat the face with clean fingertips until the remaining serum is fully absorbed. No need to rinse.

Which are Freeze 24 7 Anti Gravity Lifting Face Mask UNII Codes?

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

Which are Freeze 24 7 Anti Gravity Lifting Face Mask 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".