NDC 60687-714 Chlorhexidine Gluconate, 0.12% Oral Rinse
Solution Dental

Product Information

What is NDC 60687-714?

The NDC code 60687-714 is assigned by the FDA to the product Chlorhexidine Gluconate, 0.12% Oral Rinse which is a human prescription drug product labeled by American Health Packaging. The product's dosage form is solution and is administered via dental form. The product is distributed in 2 packages with assigned NDC codes 60687-714-16 10 tray in 1 case / 10 cup, unit-dose in 1 tray (60687-714-50) / 15 ml in 1 cup, unit-dose (60687-714-44), 60687-714-64 4 tray in 1 case / 10 cup, unit-dose in 1 tray (60687-714-50) / 15 ml in 1 cup, unit-dose (60687-714-44). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code60687-714
Proprietary Name 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.
Chlorhexidine Gluconate, 0.12% Oral Rinse
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.
Chlorhexidine Gluconate, 0.12% Oral Rinse
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.
Human Prescription Drug
Dosage FormSolution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Dental - Administration to a tooth or teeth.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
American Health Packaging
Labeler Code60687
FDA Application Number What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Marketing Category What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for Chlorhexidine Gluconate, 0.12% Oral Rinse?

Product Characteristics

Color(s)BLUE (C48333)
Flavor(s)MINT (C73404)

Product Packages

NDC Code 60687-714-16

Package Description: 10 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY (60687-714-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-714-44)

NDC Code 60687-714-64

Package Description: 4 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY (60687-714-50) / 15 mL in 1 CUP, UNIT-DOSE (60687-714-44)

Product Details

What are Chlorhexidine Gluconate, 0.12% Oral Rinse Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Chlorhexidine Gluconate, 0.12% Oral Rinse Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

Chlorhexidine Gluconate, 0.12% Oral Rinse Inactive Ingredients UNII Codes

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.

Pharmacologic Class(es)

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

* Please review the disclaimer below.

Chlorhexidine Gluconate, 0.12% Oral Rinse Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Packaging Information

American Health Packaging unit dose cups (see How Supplied section) contain drug product from Bajaj Medical as follows:
(15 ml / 40 UD) NDC 60687‐714‐64 packaged from NDC 61037‐469
(15 ml / 100 UD) NDC 60687‐714‐16 packaged from NDC 61037‐469

Distributed by:
American Health Packaging
Columbus, OH 43217


Package/Label Display Panel - Label


Rx Only


Store at 20° to 25°C (68° to 77°F); excursions
permitted between 15° to 30°C (59° to 86°F)
[see USP Controlled Room Temperature].

DIRECTIONS FOR USE: Swish in mouth undiluted
for 30 seconds, then spit out.

NOTE: To minimize medicinal taste, do not rinse with
water immediately after use.

INGREDIENTS: 0.12% chlorhexidine gluconate in a base
containing water, 11.6% alcohol, glycerin, PEG-40
sorbitan diisostearate, flavor, sodium saccharin and
FD&C Blue No. 1.



Package/Label Display Panel – Cup – 0.12%

Rx Only

NDC 60687- 714-44


Alcohol 11.6%
Delivers 15 mL

See package insert for full
prescribing information and storage.

For Institutional Use Only.

American Health Packaging
Columbus, OH 43217


* Please review the disclaimer below.