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  4. NDC Product Code: 63550-811 Sunbar Spf 30

NDC 63550-811 Sunbar Spf 30

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63550-811?
  4. Sunbar Spf 30 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:
63550-811
Proprietary Name:
Sunbar Spf 30
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kamins Dermatologics Inc.
Labeler Code:
63550
Product Label ID:
e1e056bd-1bf2-4b84-8af1-faabd24c653e
Start Marketing Date: [9]
10-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 63550-811?

The NDC code 63550-811 is assigned by the FDA to the product Sunbar Spf 30 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 63550-811-10 120 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 Sunbar Spf 30?

This oil and fragrance-free broad spectrum UVA/UVB sunscreen provides important protection against the sun’s harmful rays. Recommended for use on face and body, for everyday wear and outdoor activities. This cosmetically elegant formula is non-greasy, leaves a matte finish, and can be reapplied over makeup.• fragrance-free • oil-free• for face and bodyUses■ Helps prevent sunburn.■ Higher SPF gives more sunburn protection.■ Provides high protection against sunburn.

Which are Sunbar Spf 30 UNII Codes?

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

Which are Sunbar Spf 30 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".