NDC 69299-202 Dr. Throwers Beta

Product Information

What is NDC 69299-202?

The NDC code 69299-202 is assigned by the FDA to the product Dr. Throwers Beta which is product labeled by Dr. Thrower's Skincare, Inc.. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 69299-202-22 56 g in 1 jar . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code69299-202
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		Dr. Throwers Beta
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Dr. Thrower's Skincare, Inc.
Labeler Code69299
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		05-15-2015
Listing Expiration Date 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.		12-31-2017
Exclude Flag 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". 		I
NDC Code Structure

Product Packages

NDC Code 69299-202-22

Package Description: 56 g in 1 JAR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Dr. Throwers Beta Active Ingredients UNII Codes

Dr. Throwers Beta 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.

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Dr. Throwers Beta Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Directions:



USE AS DIRECTED. STOP USE IF REDNESS, IRRITATION, ITCHING AND/OR DARKENING OCCURS.


Ingredients:



VEGETABLE OIL, PRUNUS AMYGDALUS OIL, HYDROGENATED VEGETABLE OIL, CAMEMILLIA SINENSIS LEAF POWDER, COCOS NUCIFERA OIL / ALOE BARBEDENSIS LEAF EXTRACT, THEOBROMA CACAO SEED BUTTER, ARGENIA SPINOSA (ARGAN) OIL, CALOPHYLLUM TACAMAHACA SEED OIL, RICINUS COMMUNIS SEED OIL, BISABOLOL, FRAGRANCE


Warnings



FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. FEDERAL LAW PROHIBITS THE TRANSFER OF THIS DRUG TO ANY OTHER PERSON OTHER THAN FOR WHOM PRESCRIBED.


* Please review the disclaimer below.