NDC 50051-0005 Goofy Sun Smacker Spf 24 Berry Goal

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:
50051-0005
Proprietary Name:
Goofy Sun Smacker Spf 24 Berry Goal
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bonne Bell Llc
Labeler Code:
50051
Start Marketing Date: [9]
09-06-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
BERRY (C73365 - BERRY)

Product Packages

NDC Code 50051-0005-4

Package Description: 4 g in 1 CYLINDER

Product Details

What is NDC 50051-0005?

The NDC code 50051-0005 is assigned by the FDA to the product Goofy Sun Smacker Spf 24 Berry Goal which is product labeled by Bonne Bell Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50051-0005-4 4 g in 1 cylinder . 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 Goofy Sun Smacker Spf 24 Berry Goal?

Apply liberally 15 minutes before sun exposureUse a water resistant sunscreen if swimming or sweatingReapply at least every 2 hoursChildren under 6 months of age: Ask a doctor.

Which are Goofy Sun Smacker Spf 24 Berry Goal UNII Codes?

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

Which are Goofy Sun Smacker Spf 24 Berry Goal 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".