Product NDC: | 63433-122 |
Proprietary Name: | DHC Body Sunscreen Milk |
Non Proprietary Name: | Titanium Dioxide |
Active Ingredient(s): | 210 mg/2mL & nbsp; Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63433-122 |
Labeler Name: | DHC USA Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090401 |
Package NDC: | 63433-122-33 |
Package Description: | 1.77 mL in 1 CELLO PACK (63433-122-33) |
NDC Code | 63433-122-33 |
Proprietary Name | DHC Body Sunscreen Milk |
Package Description | 1.77 mL in 1 CELLO PACK (63433-122-33) |
Product NDC | 63433-122 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Titanium Dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090401 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | DHC USA Incorporated |
Substance Name | TITANIUM DIOXIDE |
Strength Number | 210 |
Strength Unit | mg/2mL |
Pharmaceutical Classes |