| 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 |