Product NDC: | 46414-8888 |
Proprietary Name: | Benzoin |
Non Proprietary Name: | Benzoin |
Active Ingredient(s): | .12; .6; .48; .24 g/.12mL; g/.6mL; g/.48mL; g/.24mL & nbsp; Benzoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SWAB |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 46414-8888 |
Labeler Name: | James Alexander Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19761025 |
Package NDC: | 46414-8888-2 |
Package Description: | 60 mL in 1 BOX (46414-8888-2) |
NDC Code | 46414-8888-2 |
Proprietary Name | Benzoin |
Package Description | 60 mL in 1 BOX (46414-8888-2) |
Product NDC | 46414-8888 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzoin |
Dosage Form Name | SWAB |
Route Name | TOPICAL |
Start Marketing Date | 19761025 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | James Alexander Corporation |
Substance Name | ALOE; BENZOIN; LIQUIDAMBAR STYRACIFLUA RESIN; TOLU BALSAM |
Strength Number | .12; .6; .48; .24 |
Strength Unit | g/.12mL; g/.6mL; g/.48mL; g/.24mL |
Pharmaceutical Classes |