Product NDC: | 76509-001 |
Proprietary Name: | MAXRELIEF |
Non Proprietary Name: | ARNICA MONTANA FLOWER |
Active Ingredient(s): | 50; 6; 110 mg/120mL; mg/120mL; mg/120mL & nbsp; ARNICA MONTANA FLOWER |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76509-001 |
Labeler Name: | Natures Investment Holdings Pty Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120101 |
Package NDC: | 76509-001-01 |
Package Description: | 120 mL in 1 BOTTLE, SPRAY (76509-001-01) |
NDC Code | 76509-001-01 |
Proprietary Name | MAXRELIEF |
Package Description | 120 mL in 1 BOTTLE, SPRAY (76509-001-01) |
Product NDC | 76509-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ARNICA MONTANA FLOWER |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20120101 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Natures Investment Holdings Pty Ltd |
Substance Name | ARNICA MONTANA FLOWER; EUCALYPTUS OIL; ROSEMARY OIL |
Strength Number | 50; 6; 110 |
Strength Unit | mg/120mL; mg/120mL; mg/120mL |
Pharmaceutical Classes |