70796-004 NDC - PURITON FIRST AID ANTISEPTIC AND ANTIBIOTIC SOLUTION (SILICEA, SULPHUR, PHOSPHORUS, CALCAREA SILICATA, NATRUM NITRICUM, FERRUM MURIATICUM, KALI SILICATUM)

Drug Information

Product NDC: 70796-004

Proprietary Name: Puriton FIRST AID ANTISEPTIC AND ANTIBIOTIC Solution

Non Proprietary Name: Silicea, Sulphur, Phosphorus, Calcarea Silicata, Natrum Nitricum, Ferrum Muriaticum, Kali Silicatum

Active Ingredient(s):
  • 4 [hp_X]/59mL SILICON DIOXIDE;
  • 4 [hp_X]/59mL SULFUR;
  • 6 [hp_X]/59mL PHOSPHORUS;
  • 5 [hp_X]/59mL CALCIUM SILICATE;
  • 4 [hp_X]/59mL SODIUM NITRATE;
  • 7 [hp_X]/59mL FERRIC CHLORIDE HEXAHYDRATE;
  • 6 [hp_X]/59mL POTASSIUM SILICATE


Administration Route(s): TOPICAL

Dosage Form(s): SPRAY

Labeler Information

Labeler Name: Kadesh, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/1/2017

Package Information

No. Package Code Package Description Billing Unit
170796-004-021 BOTTLE in 1 CARTON (70796-004-02) > 59 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC70796-004The 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 NAMEPuriton FIRST AID ANTISEPTIC AND ANTIBIOTIC SolutionThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESilicea, Sulphur, Phosphorus, Calcarea Silicata, Natrum Nitricum, Ferrum Muriaticum, Kali SilicatumThe 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 NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/1/2017This 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 NAMEKadesh, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMESILICON DIOXIDE; SULFUR; PHOSPHORUS; CALCIUM SILICATE; SODIUM NITRATE; FERRIC CHLORIDE HEXAHYDRATE; POTASSIUM SILICATEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH4; 4; 6; 5; 4; 7; 6 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 

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This page was last updated on: 9/13/2019