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CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE
CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE - 58668-5061-1 - (ALUMINUM CHLOROHYDRATE)
Drug Information of CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE
| Product NDC: | 58668-5061 |
| Proprietary Name: | CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 18 g/100g & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE
| Product NDC: | 58668-5061 |
| Labeler Name: | Laboratoires Clarins S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130506 |
Package Information of CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE
| Package NDC: | 58668-5061-1 |
| Package Description: | 1 CONTAINER in 1 CARTON (58668-5061-1) > 75 g in 1 CONTAINER |
NDC Information of CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE
| NDC Code | 58668-5061-1 |
| Proprietary Name | CLARINSMEN Antiperspirant ALL DAY DRY ALCOHOL-FREE |
| Package Description | 1 CONTAINER in 1 CARTON (58668-5061-1) > 75 g in 1 CONTAINER |
| Product NDC | 58668-5061 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20130506 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratoires Clarins S.A. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 18 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
