Spascupreel
NDC 50114-6129

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 50114-6129?
  4. Spascupreel 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.

Spascupreel is a UNAPPROVED HOMEOPATHIC-approved product labeled by Heel Inc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 50114-6129 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
50114-6129
Proprietary Name:
Spascupreel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Heel Inc
Labeler Code:
50114
Product Label ID:
93bd169a-7456-431d-8224-9194911058c6
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
01-31-1993
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 50114-6129?

The NDC code 50114-6129 is assigned by the FDA to the product Spascupreel. This pharmaceutical product is labeled by Heel Inc and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 50114-6129-6. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Indications: For the temporary relief of muscle spasms anywhere in the body such as:Abdominal crampsMenstrual crampsSpasmodic coughIntestinal colic

Which are the associated UNII Codes?

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

  • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
  • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
  • AMMONIUM BROMIDE (UNII: R0JB3224WS)
  • AMMONIUM BROMIDE (UNII: R0JB3224WS) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • ATROPINE SULFATE (UNII: 03J5ZE7KA5)
  • SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
  • PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
  • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
  • PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
  • PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
  • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
  • AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037)
  • AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY (UNII: DIF093I037) (Active Moiety)
  • CUPRIC SULFATE (UNII: LRX7AJ16DT)
  • CUPRIC CATION (UNII: 8CBV67279L) (Active Moiety)

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".