Triflora - 53499-5290-8 - (Symphytum Officinale, Rhus Toxicodendron, Ledum Palustre)

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Drug Information of Triflora

Product NDC: 53499-5290
Proprietary Name: Triflora
Non Proprietary Name: Symphytum Officinale, Rhus Toxicodendron, Ledum Palustre
Active Ingredient(s): 1; 1; 3    [hp_X]/78g; [hp_X]/78g; [hp_X]/78g & nbsp;   Symphytum Officinale, Rhus Toxicodendron, Ledum Palustre
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Triflora

Product NDC: 53499-5290
Labeler Name: Natures Way Holding Co.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060101

Package Information of Triflora

Package NDC: 53499-5290-8
Package Description: 1 TUBE in 1 CARTON (53499-5290-8) > 78 g in 1 TUBE

NDC Information of Triflora

NDC Code 53499-5290-8
Proprietary Name Triflora
Package Description 1 TUBE in 1 CARTON (53499-5290-8) > 78 g in 1 TUBE
Product NDC 53499-5290
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Symphytum Officinale, Rhus Toxicodendron, Ledum Palustre
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20060101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natures Way Holding Co.
Substance Name COMFREY ROOT; LEDUM PALUSTRE TWIG; TOXICODENDRON PUBESCENS LEAF
Strength Number 1; 1; 3
Strength Unit [hp_X]/78g; [hp_X]/78g; [hp_X]/78g
Pharmaceutical Classes

Complete Information of Triflora


General Information