NDC 10956-813 Reeses Onetab Cold And Flu

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:
10956-813
Proprietary Name:
Reeses Onetab Cold And Flu
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reese Pharmaceutical Co.
Labeler Code:
10956
Start Marketing Date: [9]
04-05-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

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

Product Packages

NDC Code 10956-813-01

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 30 TABLET in 1 BOTTLE, PLASTIC (10956-813-30)

Product Details

What is NDC 10956-813?

The NDC code 10956-813 is assigned by the FDA to the product Reeses Onetab Cold And Flu which is product labeled by Reese Pharmaceutical Co.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10956-813-01 1 bottle, plastic in 1 carton / 30 tablet in 1 bottle, plastic (10956-813-30). 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 Reeses Onetab Cold And Flu?

Temporarily relieves symptoms associated with the common cold, flu, hay fever and other respiratory allergiesnasal and sinus congestion itching of the nose or throatminor aches and painssneezing and runny noseitchy, watery eyesheadaches

Which are Reeses Onetab Cold And Flu UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Reeses Onetab Cold And Flu?

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: 1147619 - acetaminophen 650 MG / diphenhydrAMINE HCl 25 MG / phenylephrine HCl 10 MG Oral Tablet
  • RxCUI: 1147619 - acetaminophen 650 MG / diphenhydramine hydrochloride 25 MG / phenylephrine hydrochloride 10 MG Oral Tablet
  • RxCUI: 1147619 - APAP 650 MG / diphenhydramine hydrochloride 25 MG / phenylephrine hydrochloride 10 MG Oral Tablet

* 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".