NDC 75826-128 Phenohytro
Phenobarbital,Hyoscyamine Sulfate,Atropine Sulfate,And Scopolamine Hydrobromide Elixir - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 75826 - Winder Laboratories Llc
- 75826-128 - Phenohytro
Product Characteristics
Product Packages
NDC Code 75826-128-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC
NDC Code 75826-128-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 75826-128?
What are the uses for Phenohytro?
What are Phenohytro Active Ingredients?
- ATROPINE SULFATE .0194 mg/5mL - An alkaloid, originally from Atropa belladonna, but found in other plants, mainly SOLANACEAE. Hyoscyamine is the 3(S)-endo isomer of atropine.
- HYOSCYAMINE SULFATE .1037 mg/5mL
- PHENOBARBITAL 16.2 mg/5mL - A barbituric acid derivative that acts as a nonselective central nervous system depressant. It potentiates GAMMA-AMINOBUTYRIC ACID action on GABA-A RECEPTORS, and modulates chloride currents through receptor channels. It also inhibits glutamate induced depolarizations.
- SCOPOLAMINE HYDROBROMIDE .0065 mg/5mL
Which are Phenohytro UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENOBARBITAL (UNII: YQE403BP4D)
- PHENOBARBITAL (UNII: YQE403BP4D) (Active Moiety)
- HYOSCYAMINE SULFATE (UNII: F2R8V82B84)
- HYOSCYAMINE (UNII: PX44XO846X) (Active Moiety)
- ATROPINE SULFATE (UNII: 03J5ZE7KA5)
- ATROPINE (UNII: 7C0697DR9I) (Active Moiety)
- SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB)
- SCOPOLAMINE (UNII: DL48G20X8X) (Active Moiety)
Which are Phenohytro 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
- SUCROSE (UNII: C151H8M554)
- SORBITOL (UNII: 506T60A25R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- MINT (UNII: FV98Z8GITP)
What is the NDC to RxNorm Crosswalk for Phenohytro?
- RxCUI: 1046787 - PHENobarbital 16.2 MG / hyoscyamine sulfate 0.1037 MG / atropine sulfate 0.0194 MG / scopolamine HBr 0.0065 MG in 5 mL Oral Solution
- RxCUI: 1046787 - atropine sulfate 0.00388 MG/ML / hyoscyamine sulfate 0.0207 MG/ML / phenobarbital 3.24 MG/ML / scopolamine hydrobromide 0.0013 MG/ML Oral Solution
- RxCUI: 1046787 - atropine sulfate 0.0194 MG / hyoscyamine sulfate 0.1037 MG / phenobarbital 16.2 MG / scopolamine hydrobromide 0.0065 MG per 5 ML Oral Solution
- RxCUI: 2048017 - Phenohytro 16.2 MG / 0.1037 MG / 0.0194 MG / 0.0065 MG in 5 mL Oral Solution
- RxCUI: 2048017 - atropine sulfate 0.00388 MG/ML / hyoscyamine sulfate 0.0207 MG/ML / phenobarbital 3.24 MG/ML / scopolamine hydrobromide 0.0013 MG/ML Oral Solution [Phenohytro]
Which are the Pharmacologic Classes for Phenohytro?
- Anticholinergic - [EPC] (Established Pharmacologic Class)
- Anticholinergic - [EPC] (Established Pharmacologic Class)
- Cholinergic Antagonists - [MoA] (Mechanism of Action)
- Cholinergic Muscarinic Antagonist - [EPC] (Established Pharmacologic Class)
- Cholinergic Muscarinic Antagonists - [MoA] (Mechanism of Action)
* Please review the disclaimer below.
Patient Education
Belladonna Alkaloid Combinations and Phenobarbital
Belladonna alkaloid combinations and phenobarbital are used to relieve cramping pains in conditions such as irritable bowel syndrome and spastic colon. They also are used with other medicine to treat ulcers. These medicines decrease the motion of the stomach and intestines and the secretion of stomach fluids, including acid. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* 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.
[7] What is the Drug Enforcement Administration (DEA) CIV Schedule? - This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.
[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".