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REVITEALIZE
REVITEALIZE - 54866-000-01 - (SALICYLIC ACID)
Drug Information of REVITEALIZE
| Product NDC: | 54866-000 |
| Proprietary Name: | REVITEALIZE |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 18 mg/mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SHAMPOO |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of REVITEALIZE
| Product NDC: | 54866-000 |
| Labeler Name: | Camellix, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111201 |
Package Information of REVITEALIZE
| Package NDC: | 54866-000-01 |
| Package Description: | 250 mL in 1 BOTTLE, PLASTIC (54866-000-01) |
NDC Information of REVITEALIZE
| NDC Code | 54866-000-01 |
| Proprietary Name | REVITEALIZE |
| Package Description | 250 mL in 1 BOTTLE, PLASTIC (54866-000-01) |
| Product NDC | 54866-000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | SHAMPOO |
| Route Name | TOPICAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Camellix, LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | 18 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
