Good Neighbor Sore Throat Cherry Flavor

Phenol


Amerisource Bergen
Human Otc Drug
NDC 46122-748
Good Neighbor Sore Throat Cherry Flavor also known as Phenol is a human otc drug labeled by 'Amerisource Bergen'. National Drug Code (NDC) number for Good Neighbor Sore Throat Cherry Flavor is 46122-748. This drug is available in dosage form of Spray. The names of the active, medicinal ingredients in Good Neighbor Sore Throat Cherry Flavor drug includes Phenol - 1.4 g/100mL . The currest status of Good Neighbor Sore Throat Cherry Flavor drug is Active.

Drug Information:

Drug NDC: 46122-748
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Good Neighbor Sore Throat Cherry Flavor
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: Good Neighbor Sore Throat
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: Cherry Flavor
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Phenol
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Amerisource Bergen
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Spray
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:PHENOL - 1.4 g/100mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: OTC MONOGRAPH NOT FINAL
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 23 Jan, 2023
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 09 May, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: part356
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2024
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:AMERISOURCE BERGEN
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:198776
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0087701435317
UPC stands for Universal Product Code.
UNII:339NCG44TV
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
46122-748-76177 mL in 1 BOTTLE, SPRAY (46122-748-76)23 Jan, 2023N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Purpose oral pain reliever

Product Elements:

Good neighbor sore throat cherry flavor phenol phenol phenol fd&c red no. 40 glycerin water sucralose

Indications and Usage:

Uses for the temporarily relief of occasional minor irritation, pain, sore mouth, and sore throat.

Warnings:

Warnings sore throat warning: severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. consult a doctor promptly. do not use more than 2 days or administer to children under 6 years of age unless directed by a doctor. when using this product, do not exceed recommended dosage. stop use and ask a dentist or doctor if ▪ sore mouth symptoms do not improve in 7 days ▪ irritation, pain or redness persists or worsens ▪ swelling, rash or fever develops if pregnant or breast-feeding, ask a heath professional before use. keep out of reach of children. if more than used for minor mouth or throat pain is accidentally swallowed, get medical help or contact a poison control center right away at 1-800-222-1222

When Using:

When using this product, do not exceed recommended dosage.

Dosage and Administration:

Directions ▪ adults and children 12 years of age and older apply to affected area (one spray). allow to remain in place for at least 15 seconds, then spit out

Stop Use:

Stop use and ask a dentist or doctor if ▪ sore mouth symptoms do not improve in 7 days ▪ irritation, pain or redness persists or worsens ▪ swelling, rash or fever develops

Package Label Principal Display Panel:

Principal display panel good neighbor pharmacy® compare to chloraseptic® active ingredient* ndc# 46122-748-76 sore throat spray phenol/oral pain reliever fast acting numbs on contact sugar-free aspirin-free natural cherry flavor 6 fl oz (177 ml) *this product is not manufactured or distributed by prestige brands, inc., distributor of chloraseptic®. tamper evident: do not use if imprinted shrink band is broken or missing distributed by: amerisourcebergen 1 west first avenue conshohocken pa 19428 questions or concerns? www.mygnp.com abc sore throat phenol cherry flavor

Further Questions:

Questions or comments? 1- 866-467-2748


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.