Product NDC: | 51706-201 |
Proprietary Name: | Bodycology |
Non Proprietary Name: | Ethyl Alcohol |
Active Ingredient(s): | 65 mL/100mL & nbsp; Ethyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51706-201 |
Labeler Name: | Landy International |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100625 |
Package NDC: | 51706-201-02 |
Package Description: | 1 BOTTLE in 1 BOX (51706-201-02) > 30 mL in 1 BOTTLE (51706-201-01) |
NDC Code | 51706-201-02 |
Proprietary Name | Bodycology |
Package Description | 1 BOTTLE in 1 BOX (51706-201-02) > 30 mL in 1 BOTTLE (51706-201-01) |
Product NDC | 51706-201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethyl Alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100625 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Landy International |
Substance Name | ALCOHOL |
Strength Number | 65 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |