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Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant
Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant - 42283-003-00 - (Aluminum Chlorohydrate)
Drug Information of Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant
| Product NDC: | 42283-003 |
| Proprietary Name: | Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | 10 mL/100mL & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant
| Product NDC: | 42283-003 |
| Labeler Name: | Laboratorios Genesse SL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111227 |
Package Information of Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant
| Package NDC: | 42283-003-00 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (42283-003-00) > 50 mL in 1 BOTTLE |
NDC Information of Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant
| NDC Code | 42283-003-00 |
| Proprietary Name | Lactovit Sensitive Skin Roll-On Antiperspirant Deodorant |
| Package Description | 1 BOTTLE in 1 PACKAGE (42283-003-00) > 50 mL in 1 BOTTLE |
| Product NDC | 42283-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20111227 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Laboratorios Genesse SL |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 10 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
