Product NDC: | 55328-900 |
Proprietary Name: | Salonpas DEEP Relieving |
Non Proprietary Name: | Camphor, Menthol, Methyl salicylate |
Active Ingredient(s): | 3.1; 10; 15 g/100g; g/100g; g/100g & nbsp; Camphor, Menthol, Methyl salicylate |
Administration Route(s): | PERCUTANEOUS; TOPICAL; TRANSDERMAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55328-900 |
Labeler Name: | Hisamitsu America, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130601 |
Package NDC: | 55328-900-02 |
Package Description: | 1 TUBE in 1 BOX (55328-900-02) > 78 g in 1 TUBE |
NDC Code | 55328-900-02 |
Proprietary Name | Salonpas DEEP Relieving |
Package Description | 1 TUBE in 1 BOX (55328-900-02) > 78 g in 1 TUBE |
Product NDC | 55328-900 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Camphor, Menthol, Methyl salicylate |
Dosage Form Name | GEL |
Route Name | PERCUTANEOUS; TOPICAL; TRANSDERMAL |
Start Marketing Date | 20130601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Hisamitsu America, Inc. |
Substance Name | CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE |
Strength Number | 3.1; 10; 15 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |