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Irish Spring
Irish Spring - 35000-702-05 - (Aluminum zirconium tetrachlorohydrex gly)
Drug Information of Irish Spring
| Product NDC: | 35000-702 |
| Proprietary Name: | Irish Spring |
| Non Proprietary Name: | Aluminum zirconium tetrachlorohydrex gly |
| Active Ingredient(s): | 160 mg/g & nbsp; Aluminum zirconium tetrachlorohydrex gly |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Irish Spring
| Product NDC: | 35000-702 |
| Labeler Name: | Colgate-Palmolive Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110609 |
Package Information of Irish Spring
| Package NDC: | 35000-702-05 |
| Package Description: | 14.1 g in 1 CONTAINER (35000-702-05) |
NDC Information of Irish Spring
| NDC Code | 35000-702-05 |
| Proprietary Name | Irish Spring |
| Package Description | 14.1 g in 1 CONTAINER (35000-702-05) |
| Product NDC | 35000-702 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum zirconium tetrachlorohydrex gly |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110609 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Colgate-Palmolive Company |
| Substance Name | ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY |
| Strength Number | 160 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
