Natralia - 43251-3333-6 - (CALENDULA OFFICINALIS FLOWER, CALCIUM CARBONATE, and PULSATILLA VULGARIS)

Alphabetical Index


Drug Information of Natralia

Product NDC: 43251-3333
Proprietary Name: Natralia
Non Proprietary Name: CALENDULA OFFICINALIS FLOWER, CALCIUM CARBONATE, and PULSATILLA VULGARIS
Active Ingredient(s): 3; 6; 3    [hp_X]/g; [hp_X]/g; [hp_X]/g & nbsp;   CALENDULA OFFICINALIS FLOWER, CALCIUM CARBONATE, and PULSATILLA VULGARIS
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Natralia

Product NDC: 43251-3333
Labeler Name: LaCorium Health International Pty Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20090301

Package Information of Natralia

Package NDC: 43251-3333-6
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON (43251-3333-6) > 56 g in 1 BOTTLE, DISPENSING

NDC Information of Natralia

NDC Code 43251-3333-6
Proprietary Name Natralia
Package Description 1 BOTTLE, DISPENSING in 1 CARTON (43251-3333-6) > 56 g in 1 BOTTLE, DISPENSING
Product NDC 43251-3333
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CALENDULA OFFICINALIS FLOWER, CALCIUM CARBONATE, and PULSATILLA VULGARIS
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20090301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name LaCorium Health International Pty Ltd
Substance Name CALCIUM CARBONATE; CALENDULA OFFICINALIS FLOWER; PULSATILLA VULGARIS
Strength Number 3; 6; 3
Strength Unit [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmaceutical Classes

Complete Information of Natralia


General Information