NDC 50227-2115 Topical Anesthetic Cherry

NDC Product Code 50227-2115

NDC CODE: 50227-2115

Proprietary Name: Topical Anesthetic Cherry 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.

Product Characteristics

Color(s):
RED (C48326)
Flavor(s):
CHERRY (C73375)

NDC Code Structure

  • 50227 - Patterson Dental Supply Inc

NDC 50227-2115-1

Package Description: 29.6 g in 1 JAR

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

NDC Product Information

Topical Anesthetic Cherry with NDC 50227-2115 is a product labeled by Patterson Dental Supply Inc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 238910.

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.

  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
  • SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
  • POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
  • 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: Patterson Dental Supply Inc
Labeler Code: 50227
Start Marketing Date: 02-19-1963 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".

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Topical Anesthetic Cherry Product Label Images

Topical Anesthetic Cherry 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

Ingredients

Each gram of 20% benzocaine gel contains between 180-220 mg benzocaine U.S.P., in a water soluble base of PEG 3350 U.S.P., PEG 400 U.S.P., flavor, sodium saccharin U.S.P., and FD&C Red #40.

Usual Dosage

For oral mucosal use only as directed by a dentist.

Caution

Federal law prohibits dispensing without a prescription.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. Do not use on people with known allergies to benzocaine and PABA compounds.

Storage And Handling

Store at controlled room temperature 59-86°F (15-30°C).

Other

MADE IN U.S.A.Distributed by:PATTERSON DENTAL Patterson Dental Supply, Inc.1031 Mendota Heights Road Saint Paul, MN 55120

* Please review the disclaimer below.