| Product NDC: | 53675-134 |
| Proprietary Name: | Aruba Aloe Deodorant Women |
| Non Proprietary Name: | Aluminum Chlorohydrate |
| Active Ingredient(s): | 16 g/100g & nbsp; Aluminum Chlorohydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53675-134 |
| Labeler Name: | Aruba Aloe Balm NV |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070101 |
| Package NDC: | 53675-134-01 |
| Package Description: | 58 g in 1 BOTTLE, WITH APPLICATOR (53675-134-01) |
| NDC Code | 53675-134-01 |
| Proprietary Name | Aruba Aloe Deodorant Women |
| Package Description | 58 g in 1 BOTTLE, WITH APPLICATOR (53675-134-01) |
| Product NDC | 53675-134 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum Chlorohydrate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Aruba Aloe Balm NV |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 16 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |