NDC 59779-595 Berry Breezer Throat Drops

NDC Product Code 59779-595

NDC 59779-595-25

Package Description: 25 LOZENGE in 1 BAG

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

NDC Product Information

Berry Breezer Throat Drops with NDC 59779-595 is a product labeled by Cvs Pharmacy. The generic name of Berry Breezer Throat Drops is . The product's dosage form is and is administered via form.

Labeler Name: Cvs Pharmacy

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.

  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Cvs Pharmacy
Labeler Code: 59779
Start Marketing Date: 05-18-2015 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: 12-31-2019 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’.

* Please review the disclaimer below.

Berry Breezer Throat Drops 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

Otc - Active Ingredient

Active ingredient (in each drop)Pectin 7.0 mg

Otc - Purpose

PurposeOral demulcent

Indications & Usage

Uses temporarily relieves:occasional minor mouth irritation and sore throat

Warnings

WarningsSore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. If sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

Otc - Ask Doctor

Ask a doctor before use if you have:persistent or chronic cough such as occurs with smoking, asthma, or emphysemacough accompanied by excessive phlegm (mucus)

Otc - Stop Use

Stop use and consult doctor ifcough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.sore throat is severe, or irritation, pain or redness lasts or worsenssore mouth does not improve in 7 days

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Dosage & Administration

Directionsadults and children 5 years and over - allow 1 drop to dissolve slowly in mouth. May be repeated every 2 hours as necessary or as directed by a doctor.children under 5 years - ask a doctor

Inactive Ingredient

Inactive ingredients: Artificial flavors, coconut oil, corn starch, FD&C red #40, glucose syrup, glycerin, malic acid, medium chain triglycerides, soybean oil, soy lecithin, sucrose, titanium dioxide, and water.

Otc - Questions

Questions? Or to report an adverse event call 1-800-245-2898, Monday - Friday, 9AM to 4PM EST

* Please review the disclaimer below.