NDC 49743-3003 Select Health Allergy Relief Cherry
NDC Product 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.
Drug Use Information
Drug Use InformationThe drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
- This product is used as antihistamine
Product Characteristics
Color(s):
RED (C48326)
Flavor(s):
CHERRY (C73375)
NDC Code Structure
- 49743 - Axcentria Pharmaceuticals, Llc.
- 49743-3003 - Select Health Allergy Relief
NDC 49743-3003-1
Package Description: 118 mL in 1 BOTTLE
NDC Product Information
Select Health Allergy Relief Cherry with NDC 49743-3003 is product labeled by Axcentria Pharmaceuticals, Llc.. The product's dosage form is and is administered via form.
RxNorm Crosswalk
What is RxNorm?RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.
The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:
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 - INACTIVATED, the listing data was inactivated by the FDA. 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".
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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...
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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
- Active Ingredient (In Each 5 Ml Tsp)
- Purpose
- Uses
- Do Not Use
- Ask A Doctor Before Use
- Otc - Ask Doctor/Pharmacist
- When Using This Product
- Otc - Keep Out Of Reach Of Children
- Directions
- Other Information
- Inactive Ingredients
- Questions?
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
* Please review the disclaimer below.