Arniflora - 53499-5090-8 - (ARNICA MONTANA)

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Drug Information of Arniflora

Product NDC: 53499-5090
Proprietary Name: Arniflora
Non Proprietary Name: ARNICA MONTANA
Active Ingredient(s): 1    [hp_X]/28g & nbsp;   ARNICA MONTANA
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Arniflora

Product NDC: 53499-5090
Labeler Name: Nature's Way Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110101

Package Information of Arniflora

Package NDC: 53499-5090-8
Package Description: 1 TUBE in 1 CARTON (53499-5090-8) > 78 g in 1 TUBE

NDC Information of Arniflora

NDC Code 53499-5090-8
Proprietary Name Arniflora
Package Description 1 TUBE in 1 CARTON (53499-5090-8) > 78 g in 1 TUBE
Product NDC 53499-5090
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ARNICA MONTANA
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Nature's Way Products, Inc.
Substance Name ARNICA MONTANA
Strength Number 1
Strength Unit [hp_X]/28g
Pharmaceutical Classes

Complete Information of Arniflora


General Information