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  4. NDC Product Code: 53346-1330 Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream

NDC 53346-1330 Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53346-1330?
  4. Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream 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.
NDC Product Code:
53346-1330
Proprietary Name:
Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmazeutische Fabrik Dr. Reckeweg & Co
Labeler Code:
53346
Product Label ID:
acba12e6-0e9c-4f15-92b3-07ca2f9c7622
Start Marketing Date: [9]
06-01-1986
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 53346-1330?

The NDC code 53346-1330 is assigned by the FDA to the product Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream which is product labeled by Pharmazeutische Fabrik Dr. Reckeweg & Co. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53346-1330-1 85 g in 1 jar . 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 Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream?

UsesFor the temporary relief of:Muscle and joint painSports injuries and bruising

Which are Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream UNII Codes?

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

  • CAMPHOR (NATURAL) (UNII: N20HL7Q941)
  • CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
  • ARNICA MONTANA ROOT (UNII: MUE8Y11327)
  • ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
  • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
  • ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
  • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
  • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
  • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)

Which are Dr. Reckeweg R30 Atomare Beckeron Pain Relieving Cream 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.

[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 ("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".