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  4. NDC Product Code: 58133-390 Metaderm Eczema Body And Scalp And Baby Body And Scalp

NDC 58133-390 Metaderm Eczema Body And Scalp And Baby Body And Scalp

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 58133-390?
  4. Metaderm Eczema Body And Scalp And Baby Body And Scalp Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Get all the details for National Drug Code (NDC) 58133-390 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
58133-390
Proprietary Name:
Metaderm Eczema Body And Scalp And Baby Body And Scalp
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cosmetic Specialty Labs, Inc.
Labeler Code:
58133
Product Label ID:
7393a857-80cb-64ba-e053-2991aa0a2104
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-15-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 58133-390?

The NDC code 58133-390 is assigned by the FDA to the product Metaderm Eczema Body And Scalp And Baby Body And Scalp which is product labeled by Cosmetic Specialty Labs, Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 58133-390-04 118 ml in 1 bottle, spray , 58133-390-32 950 ml in 1 bottle , 58133-390-33 950 ml in 1 bottle , 58133-390-40 118 ml in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Metaderm Eczema Body And Scalp And Baby Body And Scalp?

For scalp, part hair, hold targeted nozzle no more than 1 inch from scalp, and spray at the roots to cover the affected area. For body, hold nozzle about 6 inches from skin and spray to cover the affected area. Lightly massage into scalp or skin with fingertips, No rinsing. Repeat on all affected areas and style hair as usual. Apply liberally to dry or wet skin 2 times daily.

Which are Metaderm Eczema Body And Scalp And Baby Body And Scalp UNII Codes?

The UNII codes for the active ingredients in this product are:

  • MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
  • MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) (Active Moiety)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508)
  • SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (Active Moiety)
  • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
  • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
  • BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3)
  • BERBERIS VULGARIS FRUIT (UNII: 6XEF22AHC3) (Active Moiety)
  • CONIUM MACULATUM FRUIT (UNII: Y71WKJ3A2K)
  • CONIUM MACULATUM FRUIT (UNII: Y71WKJ3A2K) (Active Moiety)
  • RHUS SPP. WHOLE (UNII: 3U7FG9T9MW)
  • RHUS SPP. WHOLE (UNII: 3U7FG9T9MW) (Active Moiety)
  • PHYTOLACCA OCTANDRA LEAF (UNII: 0804KD28Q9)
  • PHYTOLACCA OCTANDRA LEAF (UNII: 0804KD28Q9) (Active Moiety)
  • AESCULUS HIPPOCASTANUM SEED OIL (UNII: E0M52HIR1Y)
  • AESCULUS HIPPOCASTANUM SEED OIL (UNII: E0M52HIR1Y) (Active Moiety)

Which are Metaderm Eczema Body And Scalp And Baby Body And Scalp Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".