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  4. NDC Product Code: 63736-920 Sucrets Complete Vapor Cherry

NDC 63736-920 Sucrets Complete Vapor Cherry

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63736-920?
  5. Sucrets Complete Vapor Cherry Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63736-920
Proprietary Name:
Sucrets Complete Vapor Cherry
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Insight Pharmaceuticals
Labeler Code:
63736
Product Label ID:
ba2281f1-6bf9-4267-9404-7a6910037e79
Start Marketing Date: [9]
07-31-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
19 MM
Score:
1
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 63736-920?

The NDC code 63736-920 is assigned by the FDA to the product Sucrets Complete Vapor Cherry which is product labeled by Insight Pharmaceuticals. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63736-920-18 18 lozenge in 1 canister , 63736-920-24 24 lozenge in 1 canister . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sucrets Complete Vapor Cherry?

Adults and children 2 years of age and older: Dissolve 1 lozenge slowly in the mouth. May be repeated every 2 hours as needed or as directed by a doctor or dentist.children under 2 years of age: consult a doctor or dentist.

Which are Sucrets Complete Vapor Cherry UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sucrets Complete Vapor Cherry 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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Sucrets Complete Vapor Cherry?

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:
  • RxCUI: 1038943 - dyclonine HCl 3 MG / menthol 6 MG Oral Lozenge
  • RxCUI: 1038943 - dyclonine hydrochloride 3 MG / menthol 6 MG Oral Lozenge
  • RxCUI: 1038947 - Sucrets Complete 3 MG / 6 MG Oral Lozenge
  • RxCUI: 1038947 - dyclonine hydrochloride 3 MG / menthol 6 MG Oral Lozenge [Sucrets Complete]
  • RxCUI: 1038947 - Sucrets Complete (dyclonine hydrochloride 3 MG / menthol 6 MG) Oral Lozenge

* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".