NDC 76509-700 Maxrelief Arnica
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76509 - Natures Investment Holdings Pty Ltd Dba Maxrelief Usa
- 76509-700 - Maxrelief Arnica
Product Packages
NDC Code 76509-700-01
Package Description: 70 mg in 1 JAR
Product Details
What is NDC 76509-700?
What are the uses for Maxrelief Arnica?
Which are Maxrelief Arnica UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Maxrelief Arnica 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:
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- EMU OIL (UNII: 344821WD61)
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Maxrelief Arnica?
- RxCUI: 1539330 - camphor 0.3 % Topical Cream
- RxCUI: 1539330 - camphor 3 MG/ML 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".