Product NDC: | 66077-773 |
Proprietary Name: | Instant Foam |
Non Proprietary Name: | ALCOHOL |
Active Ingredient(s): | 620 mg/g & nbsp; ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66077-773 |
Labeler Name: | Ultra-Chem Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100301 |
Package NDC: | 66077-773-26 |
Package Description: | 454 g in 1 CAN (66077-773-26) |
NDC Code | 66077-773-26 |
Proprietary Name | Instant Foam |
Package Description | 454 g in 1 CAN (66077-773-26) |
Product NDC | 66077-773 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALCOHOL |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20100301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ultra-Chem Inc. |
Substance Name | ALCOHOL |
Strength Number | 620 |
Strength Unit | mg/g |
Pharmaceutical Classes |