68466-2006 NDC - SSSSTING STOP GEL (ECHINACEA ANGUSTIFOLIA, LEDUM PALUSTRE TWIG, URTICA DIOICA,)

Drug Information

Product NDC: 68466-2006

Proprietary Name: Ssssting Stop Gel

Non Proprietary Name: Echinacea Angustifolia, Ledum Palustre Twig, Urtica Dioica,

Active Ingredient(s):
  • 1 [hp_X]/78g ECHINACEA ANGUSTIFOLIA;
  • 2 [hp_X]/78g LEDUM PALUSTRE TWIG;
  • 1 [hp_X]/78g URTICA DIOICA


Administration Route(s): TOPICAL

Dosage Form(s): GEL

Labeler Information

Labeler Name: Schwabe Mexico, S.A. de C.V.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/19/2020

Package Information

No. Package Code Package Description Billing Unit
168466-2006-41 TUBE in 1 CARTON (68466-2006-4) / 28 g in 1 TUBE
268466-2006-81 TUBE in 1 CARTON (68466-2006-8) / 78 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC68466-2006The 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 NAMESsssting Stop GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEchinacea Angustifolia, Ledum Palustre Twig, Urtica Dioica,The 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 DATE10/19/2020This 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 NAMESchwabe Mexico, S.A. de C.V.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEECHINACEA ANGUSTIFOLIA; LEDUM PALUSTRE TWIG; URTICA DIOICAAn 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; 1 
ACTIVE INGRED UNIT[hp_X]/78g; [hp_X]/78g; [hp_X]/78g 

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