NDC 11673-143 Severe Throat Sore Drops

NDC Product Code 11673-143

NDC CODE: 11673-143

Proprietary Name: Severe Throat Sore Drops 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.

Product Characteristics

Shape: RECTANGLE (C48347)
17 MM
MENTHOL (C73403)

NDC Code Structure

  • 11673 - Target Corporation Inc.

NDC 11673-143-01

Package Description: 45 PASTILLE in 1 BAG

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

NDC Product Information

Severe Throat Sore Drops with NDC 11673-143 is a product labeled by Target Corporation Inc.. The generic name of Severe Throat Sore Drops is . The product's dosage form is and is administered via form.

Labeler Name: Target Corporation Inc.

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.

  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • WATER (UNII: 059QF0KO0R)
  • ACACIA (UNII: 5C5403N26O)
  • SUCROSE (UNII: C151H8M554)

Product Labeler Information

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

Labeler Name: Target Corporation Inc.
Labeler Code: 11673
Start Marketing Date: 10-12-2019 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: 12-31-2020 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".

* Please review the disclaimer below.

Severe Throat Sore 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 PurposesMenthol 20mg Cough SuppressantOral anesthetic

Otc - Purpose

  • Temporarily relieves ocassional minor irritation and pain due to:sore throatsore mouth

Indications & Usage

  • Temporarily relieves ocassional minor irritation and pain due to:sore throatsore mouth


WarningsSore throat warning: severe or persistence sore throat accompanied or followed by high fever, headache, nausea and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

Otc - Ask Doctor

  • Ask a doctor before use if you havea severe throat accompanied by difficulty in breathing or that last more than 2 daysa sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting

Otc - Stop Use

  • Stop use and consult a doctor ifsore mouth symptons do not improve in 7 days or if irritation, pains or redness persists or worsens.

Otc - Pregnancy Or Breast Feeding

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

Otc - Keep Out Of Reach Of Children

Keep this and all drugs out of the reach of children.


In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Dosage & Administration

  • DirectionsAdults and children 12 years and over: dissolve 1 drop slowly in mouth. Repeated every 2 hours as needed or as directed by a doctor.Children under 12 years and under do not use

Other Safety Information

  • Store in a cool and dry place

Inactive Ingredient

Eucalyptus oil, FD&C Blue No.1, glucose syrup, gum arabic, sucrose

Otc - Questions

Questions? or to report and adverse event call: 1-617-848-4560Monday to Friday 9AM to 4 PM east

* Please review the disclaimer below.