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DHC
DHC - 63433-223-31 - (Titanium dioxide and Zinc oxide)
Drug Information of DHC
| Product NDC: | 63433-223 |
| Proprietary Name: | DHC |
| Non Proprietary Name: | Titanium dioxide and Zinc oxide |
| Active Ingredient(s): | 4.98; 9.66 mg/.23g; mg/.23g & nbsp; Titanium dioxide and Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DHC
| Product NDC: | 63433-223 |
| Labeler Name: | DHC USA Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120611 |
Package Information of DHC
| Package NDC: | 63433-223-31 |
| Package Description: | 40 g in 1 TUBE (63433-223-31) |
NDC Information of DHC
| NDC Code | 63433-223-31 |
| Proprietary Name | DHC |
| Package Description | 40 g in 1 TUBE (63433-223-31) |
| Product NDC | 63433-223 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide and Zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120611 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DHC USA Incorporated |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 4.98; 9.66 |
| Strength Unit | mg/.23g; mg/.23g |
| Pharmaceutical Classes |
