NDC 49546-105 Ivy-dry Super
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49546 - Ivy-dry, Inc.
- 49546-105 - Ivy-dry Super
Product Packages
NDC Code 49546-105-03
Package Description: 89 mL in 1 CANISTER
Product Details
What is NDC 49546-105?
What are the uses for Ivy-dry Super?
Which are Ivy-dry Super UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL ALCOHOL (UNII: LKG8494WBH) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
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:
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ZINC ACETATE (UNII: FM5526K07A)
- ISOCETETH-20 (UNII: O020065R7Z)
- ZINC LACTATE (UNII: 2GXR25858Y)
What is the NDC to RxNorm Crosswalk for Ivy-dry Super?
- 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.
[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".