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  4. NDC Product Code: 46122-114 Good Neighbor Pharmacy Itch Relief Extra Strength

NDC 46122-114 Good Neighbor Pharmacy Itch Relief Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 46122-114?
  4. Good Neighbor Pharmacy Itch Relief Extra Strength Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
46122-114
Proprietary Name:
Good Neighbor Pharmacy Itch Relief Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amerisourcebergen Drug Corporation
Labeler Code:
46122
Product Label ID:
4775e0b1-3841-401e-8c4f-15b7536e46a0
Start Marketing Date: [9]
10-28-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 46122-114?

The NDC code 46122-114 is assigned by the FDA to the product Good Neighbor Pharmacy Itch Relief Extra Strength which is product labeled by Amerisourcebergen Drug Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 46122-114-21 85 g 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 Itch Relief Extra Strength?

• shake well • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 2 years of age: ask a doctor • to apply to face, spray into palm of hand and gently apply

Which are Good Neighbor Pharmacy Itch Relief Extra Strength UNII Codes?

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

Which are Good Neighbor Pharmacy Itch Relief Extra Strength 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 Itch Relief Extra Strength?

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: 1053138 - diphenhydrAMINE HCl 2 % / zinc acetate 0.1 % Topical Spray
  • RxCUI: 1053138 - diphenhydramine hydrochloride 20 MG/ML / zinc acetate 1 MG/ML Topical Spray
  • RxCUI: 1053138 - diphenhydramine hydrochloride 2 % / zinc acetate 0.1 % Topical Spray

* Please review the disclaimer below.

Patient Education

Diphenhydramine


Diphenhydramine is used to relieve red, irritated, itchy, watery eyes; sneezing; and runny nose caused by hay fever, allergies, or the common cold. Diphenhydramine is also used to relieve cough caused by minor throat or airway irritation. Diphenhydramine is also used to prevent and treat motion sickness, and to treat insomnia (difficulty falling asleep or staying asleep). Diphenhydramine is also used to control abnormal movements in people who have early stage parkinsonian syndrome (a disorder of the nervous system that causes difficulties with movement, muscle control, and balance) or who are experiencing movement problems as a side effect of a medication. Diphenhydramine will relieve the symptoms of these conditions but will not treat the cause of the symptoms or speed recovery. Diphenhydramine should not be used to cause sleepiness in children. Diphenhydramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
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* 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".