NDC 24385-925 Good Neighbor Pharmacy Mucus Relief Pe PE

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
24385-925
Proprietary Name:
Good Neighbor Pharmacy Mucus Relief Pe PE
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amerisourcebergen Drug Corp
Labeler Code:
24385
Start Marketing Date: [9]
06-05-2006
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
17 MM
Imprint(s):
RCCGPE;C27
Score:
2

Product Packages

NDC Code 24385-925-71

Package Description: 1 BOTTLE in 1 CARTON / 50 TABLET in 1 BOTTLE

Price per Unit: $0.08054 per EA

Product Details

What is NDC 24385-925?

The NDC code 24385-925 is assigned by the FDA to the product Good Neighbor Pharmacy Mucus Relief Pe PE which is product labeled by Amerisourcebergen Drug Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24385-925-71 1 bottle in 1 carton / 50 tablet 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 Good Neighbor Pharmacy Mucus Relief Pe PE?

■ adults and children 12 years and over:take 1 caplet every 4 hours as needed■ children 6 to under 12 years:take 1/2 caplet every 4 hours as needed■ children under 6 years: consult a doctorDo not exceed 6 doses in a 24 hour period or as directed by a doctor.

Which are Good Neighbor Pharmacy Mucus Relief Pe PE UNII Codes?

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

Which are Good Neighbor Pharmacy Mucus Relief Pe PE 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:

What is the NDC to RxNorm Crosswalk for Good Neighbor Pharmacy Mucus Relief Pe PE?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1304111 - guaiFENesin 400 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1304111 - guaifenesin 400 MG / phenylephrine hydrochloride 10 MG Oral Tablet

* Please review the disclaimer below.

Patient Education

Guaifenesin


Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
[Learn More]


Phenylephrine


Phenylephrine is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Phenylephrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Phenylephrine is in a class of medications called nasal decongestants. It works by reducing swelling of the blood vessels in the nasal passages.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

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

[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".