Product NDC: | 0219-0203 |
Proprietary Name: | Humphreys Bendito Alcoholado |
Non Proprietary Name: | menthol |
Active Ingredient(s): | 12.5 mg/mL & nbsp; menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0219-0203 |
Labeler Name: | Humphreys Pharmacal, Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19720111 |
Package NDC: | 0219-0203-80 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (0219-0203-80) |
NDC Code | 0219-0203-80 |
Proprietary Name | Humphreys Bendito Alcoholado |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (0219-0203-80) |
Product NDC | 0219-0203 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | menthol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19720111 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Humphreys Pharmacal, Incorporated |
Substance Name | MENTHOL |
Strength Number | 12.5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |