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Roll On Anti-Perspirant Deodorant
Roll On Anti-Perspirant Deodorant - 51870-001-03 - (ALUMINUM CHLOROHYDRATE)
Drug Information of Roll On Anti-Perspirant Deodorant
| Product NDC: | 51870-001 |
| Proprietary Name: | Roll On Anti-Perspirant Deodorant |
| Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
| Active Ingredient(s): | 14 mg/100mL & nbsp; ALUMINUM CHLOROHYDRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Roll On Anti-Perspirant Deodorant
| Product NDC: | 51870-001 |
| Labeler Name: | Keefe Group |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120626 |
Package Information of Roll On Anti-Perspirant Deodorant
| Package NDC: | 51870-001-03 |
| Package Description: | 88 mL in 1 BOTTLE, WITH APPLICATOR (51870-001-03) |
NDC Information of Roll On Anti-Perspirant Deodorant
| NDC Code | 51870-001-03 |
| Proprietary Name | Roll On Anti-Perspirant Deodorant |
| Package Description | 88 mL in 1 BOTTLE, WITH APPLICATOR (51870-001-03) |
| Product NDC | 51870-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120626 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Keefe Group |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 14 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
