MAXRELIEF - 76509-001-01 - (ARNICA MONTANA FLOWER)

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Drug Information of MAXRELIEF

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)

Labeler Information of MAXRELIEF

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 Information of MAXRELIEF

Package NDC: 76509-001-01
Package Description: 120 mL in 1 BOTTLE, SPRAY (76509-001-01)

NDC Information of MAXRELIEF

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

Complete Information of MAXRELIEF


General Information