NDC 58368-002 Neorelief For Muscle Crampling And Restlessness
Topical Gel For Muscle Cramping And Restlessness Gel Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 58368-002 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.
Code Structure Chart
Product Details
What is NDC 58368-002?
What are the uses for Neorelief For Muscle Crampling And Restlessness?
What are Neorelief For Muscle Crampling And Restlessness Active Ingredients?
- ARNICA MONTANA 4 [hp_X]/g
- ARTEMISIA CINA PRE-FLOWERING TOP 8 [hp_X]/g
- ATROPA BELLADONNA ROOT 4 [hp_X]/g
- BLACK COHOSH 4 [hp_X]/g
- CAUSTICUM 4 [hp_X]/g
- FRANGULA CALIFORNICA BARK 4 [hp_X]/g
- HYPERICUM PERFORATUM 4 [hp_X]/g
- JATROPHA CURCAS SEED 8 [hp_X]/g
- LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/g
- POTASSIUM BROMIDE 4 [hp_X]/g
- POTASSIUM CARBONATE 4 [hp_X]/g
- PSEUDOGNAPHALIUM OBTUSIFOLIUM 4 [hp_X]/g
- RUTA GRAVEOLENS FLOWERING TOP 4 [hp_X]/g
- SCUTELLARIA LATERIFLORA 4 [hp_X]/g
- STRYCHNOS IGNATII SEED 4 [hp_X]/g
- TARAXACUM OFFICINALE 4 [hp_X]/g - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- VALERIAN 8 [hp_X]/g - A plant genus of the family VALERIANACEAE, order Dipsacales, subclass Asteridae, class Magnoliopsida. It is best known for the sedative use and valepotriate content of the roots. It is sometimes called Garden Heliotrope but is unrelated to true Heliotrope (HELIOTROPIUM).
- VERATRUM ALBUM ROOT 8 [hp_X]/g
Which are Neorelief For Muscle Crampling And Restlessness UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- JATROPHA CURCAS SEED (UNII: J0F5GM8LA8)
- JATROPHA CURCAS SEED (UNII: J0F5GM8LA8) (Active Moiety)
- FRANGULA CALIFORNICA BARK (UNII: 1LZ13MQR0S)
- FRANGULA CALIFORNICA BARK (UNII: 1LZ13MQR0S) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- ATROPA BELLADONNA ROOT (UNII: 6MW97Q6E8M)
- ATROPA BELLADONNA ROOT (UNII: 6MW97Q6E8M) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT)
- ARTEMISIA CINA FLOWER (UNII: 28M1820ACT) (Active Moiety)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- POTASSIUM BROMIDE (UNII: OSD78555ZM)
- BROMIDE ION (UNII: 952902IX06) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SCUTELLARIA LATERIFLORA (UNII: 7BP4DH5PDC)
- SCUTELLARIA LATERIFLORA (UNII: 7BP4DH5PDC) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
Which are Neorelief For Muscle Crampling And Restlessness 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:
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SILVER (UNII: 3M4G523W1G)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FULVIC ACID (UNII: XII14C5FXV)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCERIN (UNII: PDC6A3C0OX)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An 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.
[3] 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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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".