NDC 70797-321 Dr Talbots Infant Pain Inflamtion Relief
Arnica 12x, Bellis Perennis 12x, Calendula Officinalis 12x, Chamomilla 12x, Coffea Cruda - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70797 - Talbot�s Pharmaceuticals Family Products, Llc.
- 70797-321 - Dr Talbots Infant Pain Inflamtion Relief
Product Packages
NDC Code 70797-321-01
Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Details
What is NDC 70797-321?
What are the uses for Dr Talbots Infant Pain Inflamtion Relief?
What are Dr Talbots Infant Pain Inflamtion Relief Active Ingredients?
- ARABICA COFFEE BEAN 12 [hp_X]/118mL
- ARNICA MONTANA 12 [hp_X]/118mL
- BELLIS PERENNIS 12 [hp_X]/118mL
- CALENDULA OFFICINALIS FLOWERING TOP 12 [hp_X]/118mL
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/118mL
- HYPERICUM PERFORATUM 12 [hp_X]/118mL
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 6 [hp_X]/118mL
- MATRICARIA CHAMOMILLA 12 [hp_X]/118mL
- 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.
Which are Dr Talbots Infant Pain Inflamtion Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
Which are Dr Talbots Infant Pain Inflamtion 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:
- CONCORD GRAPE JUICE (UNII: F7039Q79LP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
Which are the Pharmacologic Classes for Dr Talbots Infant Pain Inflamtion Relief?
- Allergens - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Potassium Compounds - [CS]
- Potassium Salt - [EPC] (Established Pharmacologic Class)
- Seed Storage Proteins - [CS]
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
* 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".