NDC 27293-030 Budpack Muscle Rub
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 27293 - Budpack Inc.
- 27293-030 - Budpack
Product Packages
NDC Code 27293-030-35
Package Description: 35 g in 1 TUBE
Product Details
What is NDC 27293-030?
What are the uses for Budpack Muscle Rub?
Which are Budpack Muscle Rub UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Budpack Muscle Rub 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:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Budpack Muscle Rub?
- RxCUI: 282805 - menthol 2.5 % Topical Gel
- RxCUI: 282805 - menthol 0.025 MG/MG Topical Gel
* 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".