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Ultra dry antiperspirant
Ultra dry antiperspirant - 29500-9211-0 - (aluminum chlorhydrate)
Drug Information of Ultra dry antiperspirant
| Product NDC: | 29500-9211 |
| Proprietary Name: | Ultra dry antiperspirant |
| Non Proprietary Name: | aluminum chlorhydrate |
| Active Ingredient(s): | 11.4 g/57g & nbsp; aluminum chlorhydrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultra dry antiperspirant
| Product NDC: | 29500-9211 |
| Labeler Name: | Personal Care Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part350 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110727 |
Package Information of Ultra dry antiperspirant
| Package NDC: | 29500-9211-0 |
| Package Description: | 57 g in 1 CONTAINER (29500-9211-0) |
NDC Information of Ultra dry antiperspirant
| NDC Code | 29500-9211-0 |
| Proprietary Name | Ultra dry antiperspirant |
| Package Description | 57 g in 1 CONTAINER (29500-9211-0) |
| Product NDC | 29500-9211 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | aluminum chlorhydrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110727 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Personal Care Products |
| Substance Name | ALUMINUM CHLOROHYDRATE |
| Strength Number | 11.4 |
| Strength Unit | g/57g |
| Pharmaceutical Classes |
