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DHC Body Sunscreen Milk
DHC Body Sunscreen Milk - 63433-122-22 - (Titanium Dioxide)
Drug Information of DHC Body Sunscreen Milk
| 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) |
Labeler Information of DHC Body Sunscreen Milk
| 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 Information of DHC Body Sunscreen Milk
| Package NDC: | 63433-122-22 |
| Package Description: | 80 mL in 1 BOTTLE, PLASTIC (63433-122-22) |
NDC Information of DHC Body Sunscreen Milk
| NDC Code | 63433-122-22 |
| Proprietary Name | DHC Body Sunscreen Milk |
| Package Description | 80 mL in 1 BOTTLE, PLASTIC (63433-122-22) |
| 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 |
