55714-2263 NDC - STAGE FRIGHT - FEAR ()

Drug Information

  • Product NDC: 55714-2263
  • Proprietary Name: Stage Fright - Fear
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Newton Laboratories, Inc.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/1/2011

Package Information

No. Package Code Package Description Billing Unit
155714-2263-07.08 g in 1 BOTTLE, GLASS (55714-2263-0)
255714-2263-128.35 g in 1 BOTTLE, GLASS (55714-2263-1)
355714-2263-256.7 g in 1 BOTTLE, GLASS (55714-2263-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55714-2263The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEStage Fright - FearThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
LABELER NAMENewton Laboratories, Inc.The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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This page was last updated on: 12/6/2025