Product NDC: | 54102-000 |
Proprietary Name: | Q Health Pain Relief Spray |
Non Proprietary Name: | MENTHOL |
Active Ingredient(s): | 80 mg/mL & nbsp; MENTHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54102-000 |
Labeler Name: | QCAN International Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120913 |
Package NDC: | 54102-000-04 |
Package Description: | 1 BOTTLE in 1 CARTON (54102-000-04) > 120 mL in 1 BOTTLE |
NDC Code | 54102-000-04 |
Proprietary Name | Q Health Pain Relief Spray |
Package Description | 1 BOTTLE in 1 CARTON (54102-000-04) > 120 mL in 1 BOTTLE |
Product NDC | 54102-000 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MENTHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120913 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | QCAN International Inc. |
Substance Name | MENTHOL |
Strength Number | 80 |
Strength Unit | mg/mL |
Pharmaceutical Classes |