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Thierry Mugler Womanity Antiperspirant Roll-On Deodorant
Thierry Mugler Womanity Antiperspirant Roll-On Deodorant - 58668-0191-1 - (ALUMINUM CHLOROHYDRATE)
Drug Information of Thierry Mugler Womanity Antiperspirant Roll-On Deodorant
| Product NDC: | 58668-0191 |
| Proprietary Name: | Thierry Mugler Womanity Antiperspirant Roll-On Deodorant |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 20 mL/100mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Thierry Mugler Womanity Antiperspirant Roll-On Deodorant
| Product NDC: | 58668-0191 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110401 |
Package Information of Thierry Mugler Womanity Antiperspirant Roll-On Deodorant
| Package NDC: | 58668-0191-1 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (58668-0191-1) > 45 mL in 1 BOTTLE |
NDC Information of Thierry Mugler Womanity Antiperspirant Roll-On Deodorant
| NDC Code | 58668-0191-1 |
| Proprietary Name | Thierry Mugler Womanity Antiperspirant Roll-On Deodorant |
| Package Description | 1 BOTTLE in 1 PACKAGE (58668-0191-1) > 45 mL in 1 BOTTLE |
| Product NDC | 58668-0191 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 20 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
