NDC 70797-319 Dr Talbots Infant Cough Relief

Antimonium Tartaricum 12x, Drosera Rotundifolia 12x, Ipecacuanha 12x, Phosphorus 12x, - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
70797-319
Proprietary Name:
Dr Talbots Infant Cough Relief
Non-Proprietary Name: [1]
Antimonium Tartaricum 12x, Drosera Rotundifolia 12x, Ipecacuanha 12x, Phosphorus 12x, Rumex Crispus 12x, Spongia Tosta 12x, Sticta Pulmonaria 12x, Kali Sulphuricum 6x
Substance Name: [2]
Antimony Tartrate Ion; Drosera Rotundifolia Flowering Top; Ipecac; Phosphorus; Pulmonaria Officinalis Whole; Rumex Crispus Root; Spongia Officinalis Skeleton, Roasted
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Talbot�s Pharmaceuticals Family Products, Llc.
    Labeler Code:
    70797
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-12-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 70797-319-01

    Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE

    Product Details

    What is NDC 70797-319?

    The NDC code 70797-319 is assigned by the FDA to the product Dr Talbots Infant Cough Relief which is a human over the counter drug product labeled by Talbot�s Pharmaceuticals Family Products, Llc.. The generic name of Dr Talbots Infant Cough Relief is antimonium tartaricum 12x, drosera rotundifolia 12x, ipecacuanha 12x, phosphorus 12x, rumex crispus 12x, spongia tosta 12x, sticta pulmonaria 12x, kali sulphuricum 6x. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 70797-319-01 1 bottle in 1 carton / 118 ml in 1 bottle. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Dr Talbots Infant Cough Relief?

    This product is used as Temporarily Relieves:Dry CoughSore Throat from coughMucus Buildup & CoughChest Congestion

    What are Dr Talbots Infant Cough Relief Active Ingredients?

    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.

    Which are Dr Talbots Infant Cough Relief UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • IPECAC (UNII: 62I3C8233L)
    • IPECAC (UNII: 62I3C8233L) (Active Moiety)
    • PULMONARIA OFFICINALIS WHOLE (UNII: 483B0A2Y00)
    • PULMONARIA OFFICINALIS WHOLE (UNII: 483B0A2Y00) (Active Moiety)
    • PHOSPHORUS (UNII: 27YLU75U4W)
    • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
    • ANTIMONY TARTRATE ION (UNII: CQN5KB2U1M)
    • ANTIMONY TARTRATE ION (UNII: CQN5KB2U1M) (Active Moiety)
    • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
    • SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
    • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
    • RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
    • DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG)
    • DROSERA ROTUNDIFOLIA FLOWERING TOP (UNII: 75O014T1HG) (Active Moiety)

    Which are Dr Talbots Infant Cough 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:

    * Please review the disclaimer below.

    Product Footnotes

    [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".