Product NDC: | 61577-3216 |
Proprietary Name: | SOMBRA WARM THERAPY |
Non Proprietary Name: | MENTHOL CAMPHOR |
Active Ingredient(s): | .03; .03 g/g; g/g & nbsp; MENTHOL CAMPHOR |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61577-3216 |
Labeler Name: | SOMBRA COSMETICS INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111216 |
Package NDC: | 61577-3216-9 |
Package Description: | 5 g in 1 POUCH (61577-3216-9) |
NDC Code | 61577-3216-9 |
Proprietary Name | SOMBRA WARM THERAPY |
Package Description | 5 g in 1 POUCH (61577-3216-9) |
Product NDC | 61577-3216 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MENTHOL CAMPHOR |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20111216 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | SOMBRA COSMETICS INC. |
Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
Strength Number | .03; .03 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |