NDC 70797-320 Dr Talbots Infant Mucus Cold Relief
Eupatorium Perf 12x, Hepar Sulphuris Calcareum 12x, Kali Bichromicum 12x, Marrubium - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70797 - Talbot�s Pharmaceuticals Family Products, Llc.
- 70797-320 - Dr Talbots Infant Mucus Cold Relief
Product Packages
NDC Code 70797-320-01
Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Details
What is NDC 70797-320?
What are the uses for Dr Talbots Infant Mucus Cold Relief?
What are Dr Talbots Infant Mucus Cold Relief Active Ingredients?
- ANEMONE PULSATILLA 12 [hp_X]/118mL
- CALCIUM SULFATE ANHYDROUS 12 [hp_X]/118mL
- CALCIUM SULFIDE 12 [hp_X]/118mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 12 [hp_X]/118mL
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/118mL
- MARRUBIUM VULGARE 12 [hp_Q]/118mL - A plant genus of the LAMIACEAE family that contains marrubiin (a labdane diterpene). It is known as a traditional medicinal for sore throat.
- PHOSPHORUS 30 [hp_X]/118mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- POTASSIUM CHLORIDE 6 [hp_X]/118mL - 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.
- POTASSIUM DICHROMATE 12 [hp_X]/118mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.
- RUMEX CRISPUS ROOT 12 [hp_X]/118mL
- SAMBUCUS NIGRA FLOWERING TOP 12 [hp_X]/118mL
Which are Dr Talbots Infant Mucus Cold Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MARRUBIUM VULGARE (UNII: 7A72MUN24Z)
- MARRUBIUM VULGARE (UNII: 7A72MUN24Z) (Active Moiety)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
Which are Dr Talbots Infant Mucus Cold Relief 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)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CONCORD GRAPE JUICE (UNII: F7039Q79LP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
Which are the Pharmacologic Classes for Dr Talbots Infant Mucus Cold Relief?
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- 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".