NDC 41525-7001 The Gargle

NDC Product Code 41525-7001

NDC 41525-7001-1

Package Description: 600 mL in 1 BOTTLE

NDC 41525-7001-2

Package Description: 780 mL in 1 BOTTLE

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

NDC Product Information

The Gargle with NDC 41525-7001 is a product labeled by Pbs Co., Ltd.. The generic name of The Gargle is . The product's dosage form is and is administered via form.

Labeler Name: Pbs Co., Ltd.

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.

  • ALLANTOIN (UNII: 344S277G0Z)
  • XYLITOL (UNII: VCQ006KQ1E)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Labeler Information

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

Labeler Name: Pbs Co., Ltd.
Labeler Code: 41525
Start Marketing Date: 01-22-2015 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: 12-31-2017 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.

The Gargle Product Label Images

The Gargle 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

Sodium fluoride

Inactive Ingredient

Purified water, ethyl alcohol, allantoin, glycerin, xylitol, sodium saccharin, green tea, malic acid, lactic acid, sodium benzoate, citric acid peg-40 hydrogenated castor oil, sodium citrate, l-menthol, red ginseng ext, ulmus ext, red ginseng fragrance, mint fragrance, houttuynia ext, propolis ext

Otc - Purpose

For dental care

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

① Turn the container cap and open, pour The Gargle into the cap about 10-15ml (not to overflow the cap) andput into mouth.② Goggle it thoroughly all over the inner mouth about 10 seconds.③ After ②, in order to sterilize mouth, hold the liquid in the mouth about 30 seconds and spit out

Warnings

Do not swallow

Dosage & Administration

For oral administration

* Please review the disclaimer below.