NDC 47682-158 Medi First Plus Sinus Pain And Pressure

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:
47682-158
Proprietary Name:
Medi First Plus Sinus Pain And Pressure
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unifirst First Aid Corporation
Labeler Code:
47682
Start Marketing Date: [9]
12-30-2008
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - BLUE)
Shape:
ROUND (C48348)
Size(s):
12 MM
Imprint(s):
FR;33
Score:
1

Product Packages

NDC Code 47682-158-33

Package Description: 50 PACKET in 1 BOX / 2 TABLET in 1 PACKET

NDC Code 47682-158-48

Package Description: 125 PACKET in 1 BOX / 2 TABLET in 1 PACKET

Product Details

What is NDC 47682-158?

The NDC code 47682-158 is assigned by the FDA to the product Medi First Plus Sinus Pain And Pressure which is product labeled by Unifirst First Aid Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 47682-158-33 50 packet in 1 box / 2 tablet in 1 packet, 47682-158-48 125 packet in 1 box / 2 tablet in 1 packet. 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 Medi First Plus Sinus Pain And Pressure?

■ do not use more than directedAdults and children: (12 years and older) Take 2 tablets every 6 hours. Do not take more than 8 tablets in 24 hours. Children under 12 years: Do not give this adult strength product to children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.

Which are Medi First Plus Sinus Pain And Pressure UNII Codes?

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

Which are Medi First Plus Sinus Pain And Pressure 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 Medi First Plus Sinus Pain And Pressure?

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: 1101534 - acetaminophen 500 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1101534 - acetaminophen 500 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1101534 - APAP 500 MG / Phenylephrine Hydrochloride 5 MG Oral Tablet

* Please review the disclaimer below.

Patient Education

Acetaminophen


Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds and sore throats, toothaches, backaches, and reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.
[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".