NDC 27293-027 Budpak Medicated Anti Itch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 27293-027?
What are the uses for Budpak Medicated Anti Itch?
Which are Budpak Medicated Anti Itch UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Budpak Medicated Anti Itch 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)
- PETROLATUM (UNII: 4T6H12BN9U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- MINERAL OIL (UNII: T5L8T28FGP)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARETH-2 (UNII: V56DFE46J5)
- ALCOHOL (UNII: 3K9958V90M)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
What is the NDC to RxNorm Crosswalk for Budpak Medicated Anti Itch?
- RxCUI: 1365000 - camphor 1 % / menthol 1 % Topical Cream
- RxCUI: 1365000 - camphor 10 MG/ML / menthol 10 MG/ML Topical Cream
* 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".