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Antiperspirant
Antiperspirant - 53329-010-13 - (aluminum chlorohydrate)
Drug Information of Antiperspirant
| Product NDC: | 53329-010 |
| Proprietary Name: | Antiperspirant |
| Non Proprietary Name: | aluminum chlorohydrate |
| Active Ingredient(s): | 13 mL/100mL & nbsp; aluminum chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antiperspirant
| Product NDC: | 53329-010 |
| Labeler Name: | Medline Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Antiperspirant
| Package NDC: | 53329-010-13 |
| Package Description: | 59 mL in 1 BOTTLE, SPRAY (53329-010-13) |
NDC Information of Antiperspirant
| NDC Code | 53329-010-13 |
| Proprietary Name | Antiperspirant |
| Package Description | 59 mL in 1 BOTTLE, SPRAY (53329-010-13) |
| Product NDC | 53329-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aluminum chlorohydrate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Medline Industries, Inc. |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 13 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
