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GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30
GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30 - 54181-002-50 - (TITANIUM DIOXIDE, ZINC OXIDE)
Drug Information of GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30
| Product NDC: | 54181-002 |
| Proprietary Name: | GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30 |
| Non Proprietary Name: | TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 96; 143 mg/mL; mg/mL & nbsp; TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30
| Product NDC: | 54181-002 |
| 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 Ultra UV Sunscreen High Protection Sun For The Face SPF 30
| Package NDC: | 54181-002-50 |
| Package Description: | 1 TUBE in 1 PACKAGE (54181-002-50) > 50 mL in 1 TUBE |
NDC Information of GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30
| NDC Code | 54181-002-50 |
| Proprietary Name | GUINOT Ultra UV Sunscreen High Protection Sun For The Face SPF 30 |
| Package Description | 1 TUBE in 1 PACKAGE (54181-002-50) > 50 mL in 1 TUBE |
| Product NDC | 54181-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130311 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Guinot SAS |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 96; 143 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
