NDC 66096-709 Cough Relief Syrup
Althaea,Antimon Sulph,Antimon Tart,Bryonia,Cetraria,Chamomilla,Drosera,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 66096-709?
What are Cough Relief Syrup Active Ingredients?
- ALTHAEA OFFICINALIS ROOT 1 [hp_X]/148mL
- ANTIMONY PENTASULFIDE 12 [hp_X]/148mL
- ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/148mL - A schistosomicide possibly useful against other parasites. It has irritant emetic properties and may cause lethal cardiac toxicity among other adverse effects.
- BRYONIA ALBA ROOT 6 [hp_X]/148mL
- CETRARIA ISLANDICA SUBSP. ISLANDICA 1 [hp_X]/148mL
- DROSERA ROTUNDIFOLIA 6 [hp_X]/148mL
- ECHINACEA ANGUSTIFOLIA 1 [hp_X]/148mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- IPECAC 6 [hp_X]/148mL - A syrup made from the dried rhizomes of two different species, CEPHAELIS ipecacuanha and C. acuminata. They contain EMETINE, cephaeline, psychotrine and other ISOQUINOLINES. Ipecac syrup is used widely as an emetic acting both locally on the gastric mucosa and centrally on the chemoreceptor trigger zone.
- MATRICARIA RECUTITA 1 [hp_X]/148mL
- PLANTAGO LANCEOLATA POLLEN 1 [hp_X]/148mL
- POLYGALA SENEGA ROOT 6 [hp_X]/148mL
- POTASSIUM CHLORIDE 6 [hp_X]/148mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
- RUMEX CRISPUS ROOT 6 [hp_X]/148mL
- SPONGIA OFFICINALIS SKELETON, ROASTED 6 [hp_X]/148mL
- SUS SCROFA THYMUS 1 [hp_X]/148mL
- TRIFOLIUM PRATENSE FLOWER 1 [hp_X]/148mL
- URTICA DIOICA 1 [hp_X]/148mL - A plant species of the genus Urtica, family URTICACEAE. Roots have been used to treat PROSTATIC HYPERPLASIA. Leaves are edible after the stinging quality is eliminated by brief heating.
- VERBASCUM THAPSUS 1 [hp_X]/148mL - A plant genus of the family Scrophulariaceae.
Which are Cough Relief Syrup UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H)
- ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) (Active Moiety)
- ANTIMONY PENTASULFIDE (UNII: 1433F1I86N)
- ANTIMONY PENTASULFIDE (UNII: 1433F1I86N) (Active Moiety)
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY CATION (3+) (UNII: 069647RPT5) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1)
- CETRARIA ISLANDICA SUBSP. ISLANDICA (UNII: BJ7YPN79A1) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ)
- DROSERA ROTUNDIFOLIA (UNII: QR44N9XPJQ) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- IPECAC (UNII: 62I3C8233L)
- IPECAC (UNII: 62I3C8233L) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF)
- POLYGALA SENEGA ROOT (UNII: M7T6H7D4IF) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
- URTICA DIOICA (UNII: 710FLW4U46)
- URTICA DIOICA (UNII: 710FLW4U46) (Active Moiety)
- VERBASCUM THAPSUS (UNII: C9TD27U172)
- VERBASCUM THAPSUS (UNII: C9TD27U172) (Active Moiety)
Which are Cough Relief Syrup 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:
- ACACIA (UNII: 5C5403N26O)
- ANISE OIL (UNII: 6Y89129C8H)
- ALCOHOL (UNII: 3K9958V90M)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GLYCERIN (UNII: PDC6A3C0OX)
- CHERRY (UNII: BUC5I9595W)
- HONEY (UNII: Y9H1V576FH)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Cough Relief Syrup?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Non-Standardized Pollen Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Pollen - [CS]
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
* 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 ("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".