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