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Salonpas DEEP Relieving
Salonpas DEEP Relieving - 55328-900-02 - (Camphor, Menthol, Methyl salicylate)
Drug Information of Salonpas DEEP Relieving
| 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) |
Labeler Information of Salonpas DEEP Relieving
| 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 Information of Salonpas DEEP Relieving
| Package NDC: | 55328-900-02 |
| Package Description: | 1 TUBE in 1 BOX (55328-900-02) > 78 g in 1 TUBE |
NDC Information of Salonpas DEEP Relieving
| 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 |