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LET ME CLARIFY
LET ME CLARIFY - 49520-103-31 - (SALICYLIC ACID)
Drug Information of LET ME CLARIFY
| Product NDC: | 49520-103 |
| Proprietary Name: | LET ME CLARIFY |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 2 g/100mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LET ME CLARIFY
| Product NDC: | 49520-103 |
| Labeler Name: | mybody |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120924 |
Package Information of LET ME CLARIFY
| Package NDC: | 49520-103-31 |
| Package Description: | 5 mL in 1 TUBE (49520-103-31) |
NDC Information of LET ME CLARIFY
| NDC Code | 49520-103-31 |
| Proprietary Name | LET ME CLARIFY |
| Package Description | 5 mL in 1 TUBE (49520-103-31) |
| Product NDC | 49520-103 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120924 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | mybody |
| Substance Name | SALICYLIC ACID |
| Strength Number | 2 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
