NDC 64058-344 Biomega Cold Pain Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64058 - Concept Laboratories, Inc.
- 64058-344 - Biomega
Product Packages
NDC Code 64058-344-68
Package Description: 234 g in 1 BOTTLE
Product Details
What is NDC 64058-344?
What are the uses for Biomega Cold Pain Therapy?
Which are Biomega Cold Pain Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Biomega Cold Pain Therapy 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- ALCOHOL (UNII: 3K9958V90M)
- STARCH, CORN (UNII: O8232NY3SJ)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- LINSEED OIL (UNII: 84XB4DV00W)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- ACAI OIL (UNII: Z0W6766A2W)
- PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
- METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)
- ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- LAURYL LAURATE (UNII: GPW77G0937)
What is the NDC to RxNorm Crosswalk for Biomega Cold Pain Therapy?
- RxCUI: 1150970 - camphor 6 % / menthol 12 % Topical Cream
- RxCUI: 1150970 - camphor 60 MG/ML / menthol 120 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".