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  4. NDC Product Code: 71240-307 Dr. Talbots Oral Comfort Pack

NDC 71240-307 Dr. Talbots Oral Comfort Pack

Pain Fever Relief And Soothing Gel Kit Oral; Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71240-307?
  4. Dr. Talbots Oral Comfort Pack Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
71240-307
Proprietary Name:
Dr. Talbots Oral Comfort Pack
Non-Proprietary Name: [1]
Pain Fever Relief And Soothing Gel
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Ningbo Longwell Baby Products Co.,ltd.
    Labeler Code:
    71240
    Product Label ID:
    b728af5e-32e7-babf-e053-2995a90a821b
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    07-06-2020
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 71240-307?

    The NDC code 71240-307 is assigned by the FDA to the product Dr. Talbots Oral Comfort Pack which is a human over the counter drug product labeled by Ningbo Longwell Baby Products Co.,ltd.. The generic name of Dr. Talbots Oral Comfort Pack is pain fever relief and soothing gel. The product's dosage form is kit and is administered via oral; topical form. The product is distributed in a single package with assigned NDC code 71240-307-01 1 kit in 1 package, combination * 1 bottle in 1 container (71240-315-01) / 118 ml in 1 bottle (71240-315-04) * 15 g in 1 tube (71240-240-15). 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 Oral Comfort Pack?

    Temporarily relievesirritabilitycold chillsflu-like symptomsfeverbody achegeneral sorenessswollen glands

    Which are Dr. Talbots Oral Comfort Pack UNII Codes?

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

    • ARNICA MONTANA ROOT (UNII: MUE8Y11327)
    • ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
    • TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
    • CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
    • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
    • MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
    • COSMOS SULPHUREUS FLOWERING TOP (UNII: WKB165X336)
    • COSMOS SULPHUREUS FLOWERING TOP (UNII: WKB165X336) (Active Moiety)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q)
    • CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (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)
    • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)

    Which are Dr. Talbots Oral Comfort Pack 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:

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    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.

    [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".