D-30 Solution
NDC 58264-0030
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
D-30 (strontium salicylate, methenamine, colchicum autumnale bulb, black cohosh, arnica montana, calendula officinalis flowering top, solanum dulcamara whole, hypericum perforatum, strychnos nux-vomica seed, atropa belladonna, echinacea angustifolia, hamamelis virginiana root bark/stem bark, achillea millefolium, and toxicodendron pubescens leaf) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Dna Labs, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a solution for sublingual administration. This product entry covers the primary NDC 58264-0030 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
58264-0030
Proprietary Name:
D-30
Non-Proprietary Name: [1]
Strontium Salicylate, Methenamine, Colchicum Autumnale Bulb, Black Cohosh, Arnica Montana, Calendula Officinalis Flowering Top, Solanum Dulcamara Whole, Hypericum Perforatum, Strychnos Nux-vomica Seed, Atropa Belladonna, Echinacea Angustifolia, Hamamelis Virginiana Root Bark/stem Bark, Achillea Millefolium, And Toxicodendron Pubescens Leaf
Substance Name: [2]
Achillea Millefolium; Arnica Montana; Atropa Belladonna; Black Cohosh; Calendula Officinalis Flowering Top; Colchicum Autumnale Bulb; Echinacea Angustifolia; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum; Methenamine; Solanum Dulcamara Whole; Strontium Salicylate; Strychnos Nux-vomica Seed; Toxicodendron Pubescens Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Solution
- A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s): [4]
Sublingual - Administration beneath the tongue.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
58264
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
01-01-1990
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 58264-0030?
The NDC code 58264-0030 is assigned by the FDA to the product D-30. It is commonly known by its generic name, strontium salicylate, methenamine, colchicum autumnale bulb, black cohosh, arnica montana, calendula officinalis flowering top, solanum dulcamara whole, hypericum perforatum, strychnos nux-vomica seed, atropa belladonna, echinacea angustifolia, hamamelis virginiana root bark/stem bark, achillea millefolium, and toxicodendron pubescens leaf. This pharmaceutical product is labeled by Dna Labs, Inc. and is currently categorized as listed product. The medication is a solution administered via sublingual route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 58264-0030-1. 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?
This product is used as Stiffness in joints and muscles.
What are Active Ingredients of this product?
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.
- ACHILLEA MILLEFOLIUM 3 [hp_X]/mL - A plant genus of the family ASTERACEAE that has long been used in folk medicine for treating wounds.
- ARNICA MONTANA 3 [hp_X]/mL
- ATROPA BELLADONNA 3 [hp_X]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BLACK COHOSH 3 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 3 [hp_X]/mL
- COLCHICUM AUTUMNALE BULB 5 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X]/mL
- HYPERICUM PERFORATUM 3 [hp_X]/mL
- METHENAMINE 4 [hp_X]/mL - An anti-infective agent most commonly used in the treatment of urinary tract infections. Its anti-infective action derives from the slow release of formaldehyde by hydrolysis at acidic pH. (From Martindale, The Extra Pharmacopoeia, 30th ed, p173)
- SOLANUM DULCAMARA WHOLE 3 [hp_X]/mL
- STRONTIUM SALICYLATE 3 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 3 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 3 [hp_X]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- STRONTIUM SALICYLATE (UNII: OGF9EV99TC)
- STRONTIUM SALICYLATE (UNII: OGF9EV99TC) (Active Moiety)
- METHENAMINE (UNII: J50OIX95QV)
- METHENAMINE (UNII: J50OIX95QV) (Active Moiety)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
- COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5)
- SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes of this product?
A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
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".
