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  4. NDC Product Code: 63550-850 Sun Defense Spf 15

NDC 63550-850 Sun Defense Spf 15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63550-850?
  4. Sun Defense Spf 15 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63550-850
Proprietary Name:
Sun Defense Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kamins Dermatologics Inc.
Labeler Code:
63550
Product Label ID:
3bcbedde-42f5-40d6-99fd-7e4c88a4975b
Start Marketing Date: [9]
09-02-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63550-850-12

Package Description: 150 mL in 1 BOX

Product Details

What is NDC 63550-850?

The NDC code 63550-850 is assigned by the FDA to the product Sun Defense Spf 15 which is product labeled by Kamins Dermatologics Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63550-850-12 150 ml in 1 box . 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 Sun Defense Spf 15?

A broad spectrum UVA/UVB sunscreen to help protect the skin from sunburn. Sun Defense Spray SPF 15 is enriched with moisturizing açai oil, pomegranate extract and Bio-MapleTM compound to help skin remain hydrated. Uses■ Helps prevent sunburn.■ Higher SPF gives more sunburn protection.■ Provides high protection against sunburn.

Which are Sun Defense Spf 15 UNII Codes?

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

Which are Sun Defense Spf 15 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".