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Roll On Anti Perspirant
Roll On Anti Perspirant - 53329-069-12 - (Aluminum Chlorohydrate)
Drug Information of Roll On Anti Perspirant
| Product NDC: | 53329-069 |
| Proprietary Name: | Roll On Anti Perspirant |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | 10 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
| Product NDC: | 53329-069 |
| Labeler Name: | Medline Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070101 |
Package Information of Roll On Anti Perspirant
| Package NDC: | 53329-069-12 |
| Package Description: | 45 mL in 1 BOTTLE (53329-069-12) |
NDC Information of Roll On Anti Perspirant
| NDC Code | 53329-069-12 |
| Proprietary Name | Roll On Anti Perspirant |
| Package Description | 45 mL in 1 BOTTLE (53329-069-12) |
| Product NDC | 53329-069 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Medline Industries, Inc. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 10 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
