Product NDC: | 49681-010 |
Proprietary Name: | Lusti Therapeutic Ice Analgesic Rub |
Non Proprietary Name: | menthol, camphor |
Active Ingredient(s): | .031; .015 g/g; g/g & nbsp; menthol, camphor |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49681-010 |
Labeler Name: | JF Labs, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100324 |
Package NDC: | 49681-010-10 |
Package Description: | 284 g in 1 JAR (49681-010-10) |
NDC Code | 49681-010-10 |
Proprietary Name | Lusti Therapeutic Ice Analgesic Rub |
Package Description | 284 g in 1 JAR (49681-010-10) |
Product NDC | 49681-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | menthol, camphor |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100324 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | JF Labs, Inc. |
Substance Name | CAMPHOR (SYNTHETIC); MENTHOL |
Strength Number | .031; .015 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes |