63776-450 NDC - RELIEF (ACETYLCHOLINE CHLORIDE, PRUNUS CERASIFERA FLOWER, CLEMATIS VITALBA FLOWER, HISTAMINE, IMPATIENS GLANDULIFERA FLOWER, HELIANTHEMUM NUMMULARIUM FLOWER, SEROTONIN, ORNITHOGALUM UMBELLATUM)

Drug Information

Product NDC: 63776-450

Proprietary Name: Relief

Non Proprietary Name: acetylcholine chloride, prunus cerasifera flower, clematis vitalba flower, histamine, impatiens glandulifera flower, helianthemum nummularium flower, serotonin, ornithogalum umbellatum

Active Ingredient(s):
  • 200 [kp_C]/mL ACETYLCHOLINE CHLORIDE;
  • 200 [kp_C]/mL PRUNUS CERASIFERA FLOWER;
  • 200 [kp_C]/mL CLEMATIS VITALBA FLOWER;
  • 200 [kp_C]/mL HISTAMINE;
  • 200 [kp_C]/mL IMPATIENS GLANDULIFERA FLOWER;
  • 200 [kp_C]/mL HELIANTHEMUM NUMMULARIUM FLOWER;
  • 200 [kp_C]/mL SEROTONIN;
  • 200 [kp_C]/mL ORNITHOGALUM UMBELLATUM


Administration Route(s): ORAL

Dosage Form(s): SPRAY

Labeler Information

Labeler Name: VIATREXX BIO INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/24/2012

Package Information

No. Package Code Package Description Billing Unit
163776-450-141 BOTTLE, SPRAY in 1 BOX (63776-450-14) > 30 mL in 1 BOTTLE, SPRAY

NDC Record

Field Name Field Value Definition
PRODUCT NDC63776-450The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEacetylcholine chloride, prunus cerasifera flower, clematis vitalba flower, histamine, impatiens glandulifera flower, helianthemum nummularium flower, serotonin, ornithogalum umbellatumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE7/24/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEVIATREXX BIO INCORPORATEDName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACETYLCHOLINE CHLORIDE; PRUNUS CERASIFERA FLOWER; CLEMATIS VITALBA FLOWER; HISTAMINE; IMPATIENS GLANDULIFERA FLOWER; HELIANTHEMUM NUMMULARIUM FLOWER; SEROTONIN; ORNITHOGALUM UMBELLATUMThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH200; 200; 200; 200; 200; 200; 200; 200 
ACTIVE INGRED UNIT[kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL; [kp_C]/mL 

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This page was last updated on: 11/18/2019