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  4. NDC Product Code: 59779-044 Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication

NDC 59779-044 Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59779-044?
  5. Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59779-044
Proprietary Name:
Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy, Inc.
Labeler Code:
59779
Product Label ID:
ec5a5404-dc36-4e94-b6d9-c2ef38a2a07c
Start Marketing Date: [9]
08-25-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 59779-044?

The NDC code 59779-044 is assigned by the FDA to the product Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication which is product labeled by Cvs Pharmacy, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-044-10 10 pouch in 1 carton / 5 ml in 1 pouch. 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 Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication?

Refer to chart belowtake every 4 to 6 hoursdo not take more than 6 doses in 24 hoursChildren under 2 years of agedo not useChildren 2 to 5 years of agedo not use unless directed by a doctorChildren 6 to 11 years of age1 to 2 pre-filled spoons (12.5 mg to 25 mg)Adults and children 12 years of age and over2 to 4 pre-filled spoons (25 mg to 50 mg)

Which are Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication UNII Codes?

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

  • DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
  • DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)

Which are Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication 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 Cvs Pharmacy Pre-measured Spoon Childrens Allergy Medication?

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: 1049906 - diphenhydrAMINE HCl 12.5 MG in 5 mL Oral Solution
  • RxCUI: 1049906 - diphenhydramine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1049906 - diphenhydramine HCl 12.5 MG per 5 ML Oral Solution
  • RxCUI: 1049906 - diphenhydramine hydrochloride 25 MG per 10 ML Oral Solution
  • RxCUI: 1049906 - diphenhydramine hydrochloride 50 MG per 20 ML Oral Solution

* 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".