NDC 82073-002 Gel Relajante Cbd

059qf0ko0r

NDC Product Code 82073-002

NDC 82073-002-01

Package Description: 50 mL in 1 VIAL, GLASS

NDC Product Information

Gel Relajante Cbd with NDC 82073-002 is a a human over the counter drug product labeled by Bosem Cosmetics Sas. The generic name of Gel Relajante Cbd is 059qf0ko0r. The product's dosage form is gel and is administered via cutaneous form.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Gel Relajante Cbd Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • MENTHOL (UNII: L7T10EIP3A)
  • SUNFLOWER OIL (UNII: 3W1JG795YI)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • TABASCO PEPPER (UNII: J1M3NA843L)
  • CINNAMON BARK OIL (UNII: XE54U569EC)
  • CLOVE OIL (UNII: 578389D6D0)
  • CANNABIDIOL (UNII: 19GBJ60SN5)
  • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
  • OLIVE OIL (UNII: 6UYK2W1W1E)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Cutaneous - Administration to the skin.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bosem Cosmetics Sas
Labeler Code: 82073
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 06-21-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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