Product NDC: | 50114-5356 |
Proprietary Name: | Thuja |
Non Proprietary Name: | THUJA OCCIDENTALIS LEAFY TWIG |
Active Ingredient(s): | 12 [hp_X]/1.1mL & nbsp; THUJA OCCIDENTALIS LEAFY TWIG |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-5356 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20100301 |
Package NDC: | 50114-5356-6 |
Package Description: | 10 VIAL, GLASS in 1 CARTON (50114-5356-6) > 1.1 mL in 1 VIAL, GLASS |
NDC Code | 50114-5356-6 |
Proprietary Name | Thuja |
Package Description | 10 VIAL, GLASS in 1 CARTON (50114-5356-6) > 1.1 mL in 1 VIAL, GLASS |
Product NDC | 50114-5356 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | THUJA OCCIDENTALIS LEAFY TWIG |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20100301 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | THUJA OCCIDENTALIS LEAFY TWIG |
Strength Number | 12 |
Strength Unit | [hp_X]/1.1mL |
Pharmaceutical Classes |