Product NDC: | 63358-101 |
Proprietary Name: | LANSINOH BABY |
Non Proprietary Name: | DIMETHICONE |
Active Ingredient(s): | 4.25; 13.175; 4.675 g/85g; g/85g; g/85g & nbsp; DIMETHICONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63358-101 |
Labeler Name: | Power Line Packaging, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110101 |
Package NDC: | 63358-101-00 |
Package Description: | 85 g in 1 TUBE (63358-101-00) |
NDC Code | 63358-101-00 |
Proprietary Name | LANSINOH BABY |
Package Description | 85 g in 1 TUBE (63358-101-00) |
Product NDC | 63358-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DIMETHICONE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20110101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Power Line Packaging, Inc |
Substance Name | DIMETHICONE; LANOLIN; ZINC OXIDE |
Strength Number | 4.25; 13.175; 4.675 |
Strength Unit | g/85g; g/85g; g/85g |
Pharmaceutical Classes |