NDC 82160-368 Sorafine Cremogel

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:
82160-368
Proprietary Name:
Sorafine Cremogel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
82160
Start Marketing Date: [9]
09-12-2011
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 82160-368?

The NDC code 82160-368 is assigned by the FDA to the product Sorafine Cremogel which is product labeled by Pella Pharmaceuticals Co. Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82160-368-01 1 tube in 1 carton / 75 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 Sorafine Cremogel?

Serafine ® Cremogel is used as a moisturizing and nourishing Gel - Cream for oily and acne prone skin, it is recommended for dry and sensitive skin, eczema, flaky skin, and similar skin problems. Serafine ® Cremogel prevents skin dryness and reduces roughness, relieves itching, gives a feeling of comfort and softness. Serafine ® Cremogel is distinguished by its non-fat composition, and contains jojoba oil which is suitable for oily skin, because of the similarity between its composition and the natural oils of the skin; which gives you a wonderful feeling of softness.

Which are Sorafine Cremogel UNII Codes?

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

Which are Sorafine Cremogel 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".