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) |
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 NDC: | 67777-228-02 |
Package Description: | 144 PACKET in 1 BOX (67777-228-02) > 5 g in 1 PACKET |
NDC Code | 67777-228-02 |
Proprietary Name | Dynashield |
Package Description | 144 PACKET in 1 BOX (67777-228-02) > 5 g in 1 PACKET |
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 |