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La Prairie Cellular Blemish Control
La Prairie Cellular Blemish Control - 68026-311-15 - (SALICYLIC ACID)
Drug Information of La Prairie Cellular Blemish Control
| Product NDC: | 68026-311 |
| Proprietary Name: | La Prairie Cellular Blemish Control |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 20 mg/mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of La Prairie Cellular Blemish Control
| Product NDC: | 68026-311 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110417 |
Package Information of La Prairie Cellular Blemish Control
| Package NDC: | 68026-311-15 |
| Package Description: | 15 mL in 1 BOTTLE (68026-311-15) |
NDC Information of La Prairie Cellular Blemish Control
| NDC Code | 68026-311-15 |
| Proprietary Name | La Prairie Cellular Blemish Control |
| Package Description | 15 mL in 1 BOTTLE (68026-311-15) |
| Product NDC | 68026-311 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110417 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
