NDC 49743-3003 Select Health Allergy Relief Cherry

  1. Labeler Index
  2. Axcentria Pharmaceuticals, Llc.
  3. NDC: 49743-3003 Select Health Allergy Relief Cherry

NDC Product Code 49743-3003

NDC CODE: 49743-3003

Proprietary Name: Select Health Allergy Relief Cherry What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 49743 - Axcentria Pharmaceuticals, Llc.

NDC 49743-3003-1

Package Description: 118 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Select Health Allergy Relief Cherry with NDC 49743-3003 is a product labeled by Axcentria Pharmaceuticals, Llc.. The generic name of Select Health Allergy Relief Cherry is . The product's dosage form is and is administered via form.

Labeler Name: Axcentria Pharmaceuticals, Llc.

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)

Product Labeler Information

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

Labeler Name: Axcentria Pharmaceuticals, Llc.
Labeler Code: 49743
Start Marketing Date: 09-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

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Information for Patients

Diphenhydramine

Diphenhydramine is pronounced as (dye fen hye' dra meen)

Why is diphenhydramine medication prescribed?
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 als...
[Read More]

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Select Health Allergy Relief Cherry Product Label Images

Select Health Allergy Relief Cherry Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Drug Facts

Active Ingredient (In Each 5 Ml Tsp)

Diphenhydramine HCl 12.5 mg

Purpose

Antihistamine

Uses

  • Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:runny nosesneezingitchy, watery eyesitching of the nose or throat

Do Not Use

  • To make a child sleepywith any other product containing diphenhydramine, even one used on skin

Ask A Doctor Before Use

  • If the child has a breathing problem such as chronic bronchitisglaucomaa sodium-restricted diet

Otc - Ask Doctor/Pharmacist

Ask a doctor or pharmacist before use if the child is taking sedatives or tranquilizers

When Using This Product

  • Marked drowsiness may occursedatives and tranquilizers may increase drowsinessexcitability may occur, especially in children

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

  • Use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.take every 4 to 6 hoursdo not take more than 6 doses in 24 hourschildren under 2 years: do not usechildren 2 to 5 years: do not use unless directed by a doctorchildren 6 to 12 years: 5 to 10 mL (1 to 2 tsp)

Other Information

  • Each teaspoon contains: sodium 14 mgstore between 20 to 25°C (68 to 77°F)protect from lightstore in outer carton until contents sused.

Inactive Ingredients

Anhydrous citric acid, D&C res #33, FD&C red #40, flavors, glycerin, monoammonium glycyrrhizinate, poloxamer 407, purified water, sodium benzoate, sodium chloride, sodium citrate, sucrose

Questions?

Adverse drug event call (888) 933-3222

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