Product NDC: | 75847-7001 |
Proprietary Name: | IASO Intensive Clear Booster |
Non Proprietary Name: | SALICYLIC ACID |
Active Ingredient(s): | .003 mL/mL & nbsp; SALICYLIC ACID |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75847-7001 |
Labeler Name: | IASO Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110109 |
Package NDC: | 75847-7001-1 |
Package Description: | 35 mL in 1 BOTTLE, WITH APPLICATOR (75847-7001-1) |
NDC Code | 75847-7001-1 |
Proprietary Name | IASO Intensive Clear Booster |
Package Description | 35 mL in 1 BOTTLE, WITH APPLICATOR (75847-7001-1) |
Product NDC | 75847-7001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SALICYLIC ACID |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110109 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | IASO Inc |
Substance Name | SALICYLIC ACID |
Strength Number | .003 |
Strength Unit | mL/mL |
Pharmaceutical Classes |