NDC 46122-697 Good Neighbor Pharmacy Medicated Chest Rub

Camphor, Menthol, Eucalyptus Oil

NDC Product Code 46122-697

NDC CODE: 46122-697

Proprietary Name: Good Neighbor Pharmacy Medicated Chest Rub What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Camphor, Menthol, Eucalyptus Oil 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.

Product Characteristics

Color(s):
WHITE (C48325)

NDC Code Structure

  • 46122 - Amerisource Bergen
    • 46122-697 - Good Neighbor Pharmacy Medicated Chest Rub

NDC 46122-697-26

Package Description: 113 g in 1 JAR

NDC Product Information

Good Neighbor Pharmacy Medicated Chest Rub with NDC 46122-697 is a a human over the counter drug product labeled by Amerisource Bergen. The generic name of Good Neighbor Pharmacy Medicated Chest Rub is camphor, menthol, eucalyptus oil. The product's dosage form is ointment and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 727137.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug 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.

Good Neighbor Pharmacy Medicated Chest Rub Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • PETROLATUM (UNII: 4T6H12BN9U)
  • CEDAR LEAF OIL (UNII: BJ169U4NLG)
  • NUTMEG OIL (UNII: Z1CLM48948)
  • THYMOL (UNII: 3J50XA376E)
  • TURPENTINE OIL (UNII: C5H0QJ6V7F)
  • PARAFFIN (UNII: I9O0E3H2ZE)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Amerisource Bergen
Labeler Code: 46122
FDA Application Number: part341 What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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.

Start Marketing Date: 05-01-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Good Neighbor Pharmacy Medicated Chest Rub Product Label Images

Good Neighbor Pharmacy Medicated Chest Rub Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredients:Camphor 4.8 %Menthol 2.6%Eucalyptus oil 1.2%

Otc - Purpose

Cough suppressant & topical analgesic,Cough suppressant

Indications & Usage

  • Temporarily relieves throat and chestcough Nasal congestion due to common coldaching musclesminor aches and pains

Warnings

For external use only; avoid contact with eyes.

Do Not Use

  • By mouthIn nostrilsOn wounds or damaged skinwith tight bandages

Otc - Ask Doctor

  • Ask A doctor use if you have:asthmaexcessive phlegm (mucus)emphysemaPersistent or chronic coughcough associated with smoking

When Using This Product, Do Not

  • HeatMicrowareUse near open flameadd to hot water or any container where heating water may cause splattering and result in burns

Stop Use And Ask A Doctor If:

  • Muscle aches/pain persist more than 7 days or comes backcough lasts more than 7 days, comes back or occurs with fever, rash, or headache that lasts. These could be a sign of a serious condition.

If Pregnant Or Breastfeeding

Ask a health professional before use

Keep Out Of Reach Of Children

In case of accidental ingestion, get medical help or contact Poison Control Center (800-222-1222) right away.

Directions:

  • See important warnings abovechildren under 2 years of age, ask a doctor before using this productAdults and children 2 years and older, rub a thick layer on chest and throat or rub on sore aching muscles. If desired cover with a dry soft cloth but keep clothing loose. Repeat up to 3 times daily.

Other Information

Store at room temperature

Inactive Ingredients:

Cedar leaf oil, nutmeg oil, paraffin, petrolatum, thymol, turpentine oil.

* Please review the disclaimer below.