Product NDC: | 15197-007 |
Proprietary Name: | Bodyglide anti chafe balm |
Non Proprietary Name: | Allantoin |
Active Ingredient(s): | 5 mg/g & nbsp; Allantoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 15197-007 |
Labeler Name: | W STERNOFF LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20091124 |
Package NDC: | 15197-007-26 |
Package Description: | 1 TUBE in 1 PACKAGE (15197-007-26) > 70 g in 1 TUBE (15197-007-25) |
NDC Code | 15197-007-26 |
Proprietary Name | Bodyglide anti chafe balm |
Package Description | 1 TUBE in 1 PACKAGE (15197-007-26) > 70 g in 1 TUBE (15197-007-25) |
Product NDC | 15197-007 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Allantoin |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20091124 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | W STERNOFF LLC |
Substance Name | ALLANTOIN |
Strength Number | 5 |
Strength Unit | mg/g |
Pharmaceutical Classes |