NDC 51514-0327 Yes To Tomatoes Roller Ball Spot Stick

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:
51514-0327
Proprietary Name:
Yes To Tomatoes Roller Ball Spot Stick
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Autumn Harp, Inc.
Labeler Code:
51514
Start Marketing Date: [9]
01-12-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51514-0327-1

Package Description: 14.7 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 51514-0327?

The NDC code 51514-0327 is assigned by the FDA to the product Yes To Tomatoes Roller Ball Spot Stick which is product labeled by Autumn Harp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51514-0327-1 14.7 ml in 1 bottle, with applicator . 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 Yes To Tomatoes Roller Ball Spot Stick?

Apply Spot Stick directly on blemishes 1 - 3 times daily.  Because excessive drying of skin may occur start with one application and gradually increase as needed. 

Which are Yes To Tomatoes Roller Ball Spot Stick UNII Codes?

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

Which are Yes To Tomatoes Roller Ball Spot Stick 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:

What is the NDC to RxNorm Crosswalk for Yes To Tomatoes Roller Ball Spot Stick?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".