Product NDC: | 29500-9090 |
Proprietary Name: | Personal Care |
Non Proprietary Name: | Medicated Body Powder |
Active Ingredient(s): | 3; 20 mg/2g; mg/2g & nbsp; Medicated Body Powder |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 29500-9090 |
Labeler Name: | Personal Care Products, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090901 |
Package NDC: | 29500-9090-1 |
Package Description: | 283 g in 1 BOTTLE (29500-9090-1) |
NDC Code | 29500-9090-1 |
Proprietary Name | Personal Care |
Package Description | 283 g in 1 BOTTLE (29500-9090-1) |
Product NDC | 29500-9090 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Medicated Body Powder |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20090901 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Personal Care Products, Inc. |
Substance Name | MENTHOL; ZINC OXIDE |
Strength Number | 3; 20 |
Strength Unit | mg/2g; mg/2g |
Pharmaceutical Classes |