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DHC White Sunscreen
DHC White Sunscreen - 63433-451-79 - (Titanium Dioxide and Zinc Oxide)
Drug Information of DHC White Sunscreen
| Product NDC: | 63433-451 |
| Proprietary Name: | DHC White Sunscreen |
| Non Proprietary Name: | Titanium Dioxide and Zinc Oxide |
| Active Ingredient(s): | 50; 100 mg/g; mg/g & nbsp; Titanium Dioxide and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DHC White Sunscreen
| Product NDC: | 63433-451 |
| Labeler Name: | DHC USA Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050501 |
Package Information of DHC White Sunscreen
| Package NDC: | 63433-451-79 |
| Package Description: | 1.5 g in 1 CELLO PACK (63433-451-79) |
NDC Information of DHC White Sunscreen
| NDC Code | 63433-451-79 |
| Proprietary Name | DHC White Sunscreen |
| Package Description | 1.5 g in 1 CELLO PACK (63433-451-79) |
| Product NDC | 63433-451 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide and Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20050501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | DHC USA Incorporated |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 50; 100 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
