NDC 70797-308 Dr. Talbots Infant Daily Allergy Relief
Allium Cepa,Aralia Racemosa,Euphrasia Officinalis,Galphimia Glauca,Histaminum - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70797-308?
What are the uses for Dr. Talbots Infant Daily Allergy Relief?
What are Dr. Talbots Infant Daily Allergy Relief Active Ingredients?
- ANEMONE PULSATILLA 12 [hp_X]/118mL
- ARALIA RACEMOSA ROOT 12 [hp_X]/118mL
- EUPHRASIA STRICTA 12 [hp_X]/118mL
- GALPHIMIA GLAUCA FLOWERING TOP 12 [hp_X]/118mL
- HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/118mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
- LUFFA OPERCULATA FRUIT 12 [hp_X]/118mL
- ONION 12 [hp_X]/118mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
- SODIUM CHLORIDE 6 [hp_X]/118mL - A ubiquitous sodium salt that is commonly used to season food.
- SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]/118mL
Which are Dr. Talbots Infant Daily Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E)
- GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (Active Moiety)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU)
- ARALIA RACEMOSA ROOT (UNII: T90W4582DU) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- ONION (UNII: 492225Q21H)
- ONION (UNII: 492225Q21H) (Active Moiety)
- ANEMONE PULSATILLA (UNII: I76KB35JEV)
- ANEMONE PULSATILLA (UNII: I76KB35JEV) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
Which are Dr. Talbots Infant Daily Allergy 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)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CONCORD GRAPE JUICE (UNII: F7039Q79LP)
- WATER (UNII: 059QF0KO0R)
Which are the Pharmacologic Classes for Dr. Talbots Infant Daily Allergy Relief?
- Allergens - [CS]
- 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)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
* 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".