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SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20
SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20 - 0023-4953-02 - (octinoxate, zinc oxide)
Drug Information of SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20
| Product NDC: | 0023-4953 |
| Proprietary Name: | SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20 |
| Non Proprietary Name: | octinoxate, zinc oxide |
| Active Ingredient(s): | 75; 53 mg/g; mg/g & nbsp; octinoxate, zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20
| Product NDC: | 0023-4953 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130101 |
Package Information of SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20
| Package NDC: | 0023-4953-02 |
| Package Description: | 1 TUBE in 1 CARTON (0023-4953-02) > 56.7 g in 1 TUBE |
NDC Information of SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20
| NDC Code | 0023-4953-02 |
| Proprietary Name | SkinMedica TNS Ultimate Daily Moisturizer Sunscreen SPF 20 |
| Package Description | 1 TUBE in 1 CARTON (0023-4953-02) > 56.7 g in 1 TUBE |
| Product NDC | 0023-4953 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 75; 53 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
