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GUINOT Skin Defense SPF 15 Face
GUINOT Skin Defense SPF 15 Face - 54181-001-50 - (OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE)
Drug Information of GUINOT Skin Defense SPF 15 Face
| Product NDC: | 54181-001 |
| Proprietary Name: | GUINOT Skin Defense SPF 15 Face |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 60; 50; 40; 11 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GUINOT Skin Defense SPF 15 Face
| Product NDC: | 54181-001 |
| Labeler Name: | Guinot SAS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130311 |
Package Information of GUINOT Skin Defense SPF 15 Face
| Package NDC: | 54181-001-50 |
| Package Description: | 1 JAR in 1 PACKAGE (54181-001-50) > 50 mL in 1 JAR |
NDC Information of GUINOT Skin Defense SPF 15 Face
| NDC Code | 54181-001-50 |
| Proprietary Name | GUINOT Skin Defense SPF 15 Face |
| Package Description | 1 JAR in 1 PACKAGE (54181-001-50) > 50 mL in 1 JAR |
| Product NDC | 54181-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130311 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guinot SAS |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 60; 50; 40; 11 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
