NDC 59779-625 Throat Relief Pops

  1. Labeler Index
  2. Cvs Pharmacy
  3. NDC: 59779-625 Throat Relief Pops

NDC Product Code 59779-625

NDC CODE: 59779-625

Proprietary Name: Throat Relief Pops 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

  • 59779 - Cvs Pharmacy

NDC 59779-625-20

Package Description: 20 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

Throat Relief Pops with NDC 59779-625 is a product labeled by Cvs Pharmacy. The generic name of Throat Relief Pops 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.

Throat Relief Pops Product Label Images

Throat Relief Pops 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 pop)Pectin 10 mg

Otc - Purpose

PurposeOral demulcent

Indications & Usage

UsesFor temporary relief of minor discomfort and protection of irritated areas in sore mouth 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. These symptoms may be serious.

Otc - Stop Use

Stop use and ask doctor ifirritation, 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 3 years and over - allow 1 pop to dissolve slowly in mouth. May be repeated as necessary or as directed by a doctor.children under 3 years - ask a doctor

Other Safety Information

Not a candy

Inactive Ingredient

Inactive ingredients: Ascorbic acid, citric acid, corn starch, corn syrup, FD&C blue no. 1, FD&C red no. 40, glycerin, medium chain triglycerides, natural and artificial flavors, sodium ascorbate, soybean oil, sucrose, water and zinc gluconate.

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.