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Baby Daily Face and Body
Baby Daily Face and Body - 58232-9204-4 - (Titanium dioxide and Zinc Oxide)
Drug Information of Baby Daily Face and Body
| Product NDC: | 58232-9204 |
| Proprietary Name: | Baby Daily Face and Body |
| Non Proprietary Name: | Titanium dioxide and Zinc Oxide |
| Active Ingredient(s): | 121.7; 50 mg/mL; mg/mL & nbsp; Titanium dioxide and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Baby Daily Face and Body
| Product NDC: | 58232-9204 |
| Labeler Name: | Johnson & Johnson Consumer Products Co., Division of Johnson & Johnson Consumer Companies, inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091115 |
Package Information of Baby Daily Face and Body
| Package NDC: | 58232-9204-4 |
| Package Description: | 118 mL in 1 TUBE (58232-9204-4) |
NDC Information of Baby Daily Face and Body
| NDC Code | 58232-9204-4 |
| Proprietary Name | Baby Daily Face and Body |
| Package Description | 118 mL in 1 TUBE (58232-9204-4) |
| Product NDC | 58232-9204 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Co., Division of Johnson & Johnson Consumer Companies, inc. |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 121.7; 50 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
