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Dynashield
Dynashield - 67777-228-01 - (zinc oxide and dimethicone)
Drug Information of Dynashield
| Product NDC: | 67777-228 |
| Proprietary Name: | Dynashield |
| Non Proprietary Name: | zinc oxide and dimethicone |
| Active Ingredient(s): | 18; 200 mg/g; mg/g & nbsp; zinc oxide and dimethicone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dynashield
| Product NDC: | 67777-228 |
| Labeler Name: | Dynarex Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090901 |
Package Information of Dynashield
| Package NDC: | 67777-228-01 |
| Package Description: | 24 TUBE in 1 CARTON (67777-228-01) > 113.4 g in 1 TUBE |
NDC Information of Dynashield
| NDC Code | 67777-228-01 |
| Proprietary Name | Dynashield |
| Package Description | 24 TUBE in 1 CARTON (67777-228-01) > 113.4 g in 1 TUBE |
| Product NDC | 67777-228 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | zinc oxide and dimethicone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Dynarex Corporation |
| Substance Name | DIMETHICONE; ZINC OXIDE |
| Strength Number | 18; 200 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
