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  4. NDC Product Code: 49546-105 Ivy-dry Super

NDC 49546-105 Ivy-dry Super

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49546-105?
  4. Ivy-dry Super Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
49546-105
Proprietary Name:
Ivy-dry Super
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ivy-dry, Inc.
Labeler Code:
49546
Product Label ID:
22014fde-2648-4514-99c5-668481fa12c1
Start Marketing Date: [9]
07-11-2012
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49546-105-03

Package Description: 89 mL in 1 CANISTER

Product Details

What is NDC 49546-105?

The NDC code 49546-105 is assigned by the FDA to the product Ivy-dry Super which is product labeled by Ivy-dry, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49546-105-03 89 ml 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 Ivy-dry Super?

Apply to affected area not more than 3 times daily.Children under 6 years of age: do not use, ask a doctor.Severe reactions to Urushiol (the chemical released by the plant, which causes the irritation) can look like chemical burns and have a thick leathery appearance. Additional applications may be necessary. Test product on small patch of skin before applying to the entire body.

Which are Ivy-dry Super UNII Codes?

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

Which are Ivy-dry Super 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 Ivy-dry Super?

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: 1302630 - benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % Topical Spray
  • RxCUI: 1302630 - benzyl alcohol 0.1 ML/ML / camphor 5 MG/ML / menthol 2.5 MG/ML Topical Spray
  • RxCUI: 1302633 - IVY DRY SUPER 10 % / 0.5 % / 0.25 % Topical Spray
  • RxCUI: 1302633 - benzyl alcohol 0.1 ML/ML / camphor 5 MG/ML / menthol 2.5 MG/ML Topical Spray [Ivy Dry Super Continuous Spray]
  • RxCUI: 1302633 - Ivy Dry Super Continuous Spray (benzyl alcohol 10 % / camphor 0.5 % / menthol 0.25 % ) Topical Spray

* 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".