NDC 59667-0027 Cough And Cold

  1. Labeler Index
  2. Home Sweet Homeopathics
  3. NDC: 59667-0027 Cough And Cold

NDC Product Code 59667-0027

NDC CODE: 59667-0027

Proprietary Name: Cough And Cold 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 Information
The 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 for symptoms associated with

NDC Code Structure

NDC 59667-0027-2

Package Description: 30 [hp_C] in 1 BOTTLE, SPRAY

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

NDC Product Information

Cough And Cold with NDC 59667-0027 is product labeled by Home Sweet Homeopathics. The product's dosage form is and is administered via form.

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)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

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

Labeler Name: Home Sweet Homeopathics
Labeler Code: 59667
Start Marketing Date: 08-02-2013 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".

* Please review the disclaimer below.

Cough And Cold Product Label Images

Cough And Cold 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 - Purpose

For symptoms associated with

For Symptoms Associated With:

To be used according to label indications.

Directions:

Spritz 1 time under the tongue 3 x per day until improvement is seen, dose once each time symptoms return.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

If no improvement is seen after 7 days or new symptoms develop, discontinue use.

Active Ingredients:

Listed for each remedy.

Inactive Ingredients:

In reverse osmosis water with less than 1% alcohol.

* Please review the disclaimer below.