Product NDC: | 12745-109 |
Proprietary Name: | Compound Benzoin Tincture |
Non Proprietary Name: | Tincture of Benzoin |
Active Ingredient(s): | 10 g/100mL & nbsp; Tincture of Benzoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 12745-109 |
Labeler Name: | Medical Chemical Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19540615 |
Package NDC: | 12745-109-01 |
Package Description: | 59 mL in 1 BOTTLE (12745-109-01) |
NDC Code | 12745-109-01 |
Proprietary Name | Compound Benzoin Tincture |
Package Description | 59 mL in 1 BOTTLE (12745-109-01) |
Product NDC | 12745-109 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tincture of Benzoin |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19540615 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Medical Chemical Corporation |
Substance Name | BENZOIN RESIN |
Strength Number | 10 |
Strength Unit | g/100mL |
Pharmaceutical Classes |