Product NDC: | 10056-178 |
Proprietary Name: | Body Series Deodorant and Antiperspirant Roll-On |
Non Proprietary Name: | ALUMINUM CHLOROHYDRATE |
Active Ingredient(s): | 25 mL/100mL & nbsp; ALUMINUM CHLOROHYDRATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10056-178 |
Labeler Name: | Access Business Group, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110411 |
Package NDC: | 10056-178-10 |
Package Description: | 100 mL in 1 BOTTLE, PLASTIC (10056-178-10) |
NDC Code | 10056-178-10 |
Proprietary Name | Body Series Deodorant and Antiperspirant Roll-On |
Package Description | 100 mL in 1 BOTTLE, PLASTIC (10056-178-10) |
Product NDC | 10056-178 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALUMINUM CHLOROHYDRATE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110411 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Access Business Group, Inc. |
Substance Name | ALUMINUM CHLOROHYDRATE |
Strength Number | 25 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |