NDC 49546-201 Ivy Dry
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49546-201?
What are the uses for Ivy Dry?
Which are Ivy Dry 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 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ZINC ACETATE (UNII: FM5526K07A)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-20 (UNII: L0Q8IK9E08)
- STEARETH-100 (UNII: 4OH5W9UM87)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALLANTOIN (UNII: 344S277G0Z)
What is the NDC to RxNorm Crosswalk for Ivy Dry?
- RxCUI: 1305913 - benzyl alcohol 10 % / camphor 0.6 % / menthol 0.4 % Topical Cream
- RxCUI: 1305913 - benzyl alcohol 100 MG/ML / camphor 6 MG/ML / menthol 4 MG/ML Topical Cream
- RxCUI: 1305916 - Ivy-Dry Cream 10 % / 0.6 % / 0.4 % Topical Cream
- RxCUI: 1305916 - benzyl alcohol 100 MG/ML / camphor 6 MG/ML / menthol 4 MG/ML Topical Cream [Ivy-Dry Cream]
- RxCUI: 1305916 - Ivy-Dry Cream (benzyl alcohol 10 % / camphor 0.6 % / menthol 0.4 % ) Topical Cream
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[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".