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Becca
Becca - 23104-5010-2 - (Zinc Oxide)
Drug Information of Becca
| Product NDC: | 23104-5010 |
| Proprietary Name: | Becca |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 17 mL/100mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Becca
| Product NDC: | 23104-5010 |
| Labeler Name: | Cosmetic Developments Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100707 |
Package Information of Becca
| Package NDC: | 23104-5010-2 |
| Package Description: | 1 BOTTLE in 1 BOX (23104-5010-2) > 50 mL in 1 BOTTLE (23104-5010-1) |
NDC Information of Becca
| NDC Code | 23104-5010-2 |
| Proprietary Name | Becca |
| Package Description | 1 BOTTLE in 1 BOX (23104-5010-2) > 50 mL in 1 BOTTLE (23104-5010-1) |
| Product NDC | 23104-5010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100707 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cosmetic Developments Limited |
| Substance Name | ZINC OXIDE |
| Strength Number | 17 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
