10893-900 NDC - COBRAZOL (ARNICA MONTANA, CAPSICUM ANNUM, CROTALUS HORRIDUS, LACHESIS MUTA, NAJA TRIPUDIANS)

Drug Information

Product NDC: 10893-900

Proprietary Name: CobraZol

Non Proprietary Name: Arnica montana, Capsicum annum, Crotalus horridus, Lachesis muta, Naja tripudians

Active Ingredient(s):
  • 1 [hp_X]/88.721mL ARNICA MONTANA;
  • 2 [hp_X]/88.721mL CAPSICUM;
  • 6 [hp_X]/88.721mL CROTALUS HORRIDUS HORRIDUS VENOM;
  • 8 [hp_X]/88.721mL LACHESIS MUTA VENOM;
  • 5 [hp_X]/88.721mL NAJA NAJA VENOM


Administration Route(s): TOPICAL

Dosage Form(s): GEL

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Nature's Innovation, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/21/2013

Package Information

No. Package Code Package Description Billing Unit
110893-900-031 BOTTLE, DISPENSING in 1 PACKAGE (10893-900-03) / 88.721 mL in 1 BOTTLE, DISPENSING

NDC Record

Field Name Field Value Definition
PRODUCT NDC10893-900The 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 NAMECobraZolThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEArnica montana, Capsicum annum, Crotalus horridus, Lachesis muta, Naja tripudiansThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGELThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/21/2013This 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 NAMENature's Innovation, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARNICA MONTANA; CAPSICUM; CROTALUS HORRIDUS HORRIDUS VENOM; LACHESIS MUTA VENOM; NAJA NAJA VENOMAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH1; 2; 6; 8; 5 
ACTIVE INGRED UNIT[hp_X]/88.721mL; [hp_X]/88.721mL; [hp_X]/88.721mL; [hp_X]/88.721mL; [hp_X]/88.721mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS] 

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This page was last updated on: 2/1/2023