NDC 42507-147 Calamine Plus Pramoxine Hcl
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42507 - Hy-vee, Inc
- 42507-147 - Calamine Plus Pramoxine Hcl
Product Packages
NDC Code 42507-147-41
Package Description: 116 g in 1 CANISTER
Product Details
What is NDC 42507-147?
What are the uses for Calamine Plus Pramoxine Hcl?
Which are Calamine Plus Pramoxine Hcl UNII Codes?
The UNII codes for the active ingredients in this product are:
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE RED (UNII: 1K09F3G675) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Calamine Plus Pramoxine Hcl 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- ISOBUTANE (UNII: BXR49TP611)
- OLEYL ALCOHOL (UNII: 172F2WN8DV)
- ALCOHOL (UNII: 3K9958V90M)
- SORBITAN TRIOLEATE (UNII: QE6F49RPJ1)
What is the NDC to RxNorm Crosswalk for Calamine Plus Pramoxine Hcl?
- RxCUI: 1544717 - calamine 8 % / pramoxine HCl 1 % Topical Spray
- RxCUI: 1544717 - calamine 80 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Spray
- RxCUI: 1544717 - calamine 8 % / pramoxine hydrochloride 1 % Topical Spray
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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".