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Sunscreen Day Broad Spectrum SPF 40
Sunscreen Day Broad Spectrum SPF 40 - 75936-117-01 - (Octinoxate, Zinc Oxide)
Drug Information of Sunscreen Day Broad Spectrum SPF 40
| Product NDC: | 75936-117 |
| Proprietary Name: | Sunscreen Day Broad Spectrum SPF 40 |
| Non Proprietary Name: | Octinoxate, Zinc Oxide |
| Active Ingredient(s): | 2.25; 3.03 g/30mL; g/30mL & nbsp; Octinoxate, Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen Day Broad Spectrum SPF 40
| Product NDC: | 75936-117 |
| Labeler Name: | TAYLOR JAMES, LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120626 |
Package Information of Sunscreen Day Broad Spectrum SPF 40
| Package NDC: | 75936-117-01 |
| Package Description: | 1 TUBE in 1 BOX (75936-117-01) > 30 mL in 1 TUBE (75936-117-02) |
NDC Information of Sunscreen Day Broad Spectrum SPF 40
| NDC Code | 75936-117-01 |
| Proprietary Name | Sunscreen Day Broad Spectrum SPF 40 |
| Package Description | 1 TUBE in 1 BOX (75936-117-01) > 30 mL in 1 TUBE (75936-117-02) |
| Product NDC | 75936-117 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120626 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TAYLOR JAMES, LTD. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 2.25; 3.03 |
| Strength Unit | g/30mL; g/30mL |
| Pharmaceutical Classes |
