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CLARINS Roll-On Deodorant Anti-perspirant
CLARINS Roll-On Deodorant Anti-perspirant - 58668-5961-1 - (ALUMINUM CHLOROHYDRATE)
Drug Information of CLARINS Roll-On Deodorant Anti-perspirant
| Product NDC: | 58668-5961 |
| Proprietary Name: | CLARINS Roll-On Deodorant Anti-perspirant |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 180 mg/mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLARINS Roll-On Deodorant Anti-perspirant
| Product NDC: | 58668-5961 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130311 |
Package Information of CLARINS Roll-On Deodorant Anti-perspirant
| Package NDC: | 58668-5961-1 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (58668-5961-1) > 50 mL in 1 BOTTLE |
NDC Information of CLARINS Roll-On Deodorant Anti-perspirant
| NDC Code | 58668-5961-1 |
| Proprietary Name | CLARINS Roll-On Deodorant Anti-perspirant |
| Package Description | 1 BOTTLE in 1 PACKAGE (58668-5961-1) > 50 mL in 1 BOTTLE |
| Product NDC | 58668-5961 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130311 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 180 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
