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Irish Spring
Irish Spring - 35000-873-90 - (Salicylic acid)
Drug Information of Irish Spring
| Product NDC: | 35000-873 |
| Proprietary Name: | Irish Spring |
| Non Proprietary Name: | Salicylic acid |
| Active Ingredient(s): | 20 mL/L & nbsp; Salicylic acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Irish Spring
| Product NDC: | 35000-873 |
| Labeler Name: | Colgate-Palmolive Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120626 |
Package Information of Irish Spring
| Package NDC: | 35000-873-90 |
| Package Description: | 73.9 L in 1 BOTTLE (35000-873-90) |
NDC Information of Irish Spring
| NDC Code | 35000-873-90 |
| Proprietary Name | Irish Spring |
| Package Description | 73.9 L in 1 BOTTLE (35000-873-90) |
| Product NDC | 35000-873 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120626 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Colgate-Palmolive Company |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mL/L |
| Pharmaceutical Classes |
