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SPF 40 UVA/UVB
SPF 40 UVA/UVB - 51191-2015-1 - (titanium dioxide, octinoxate, octisalate, homosalate)
Drug Information of SPF 40 UVA/UVB
| Product NDC: | 51191-2015 |
| Proprietary Name: | SPF 40 UVA/UVB |
| Non Proprietary Name: | titanium dioxide, octinoxate, octisalate, homosalate |
| Active Ingredient(s): | 4; 7.5; 5; 11 g/100g; g/100g; g/100g; g/100g & nbsp; titanium dioxide, octinoxate, octisalate, homosalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPF 40 UVA/UVB
| Product NDC: | 51191-2015 |
| Labeler Name: | MULTALER & CIE S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110215 |
Package Information of SPF 40 UVA/UVB
| Package NDC: | 51191-2015-1 |
| Package Description: | 50 g in 1 TUBE (51191-2015-1) |
NDC Information of SPF 40 UVA/UVB
| NDC Code | 51191-2015-1 |
| Proprietary Name | SPF 40 UVA/UVB |
| Package Description | 50 g in 1 TUBE (51191-2015-1) |
| Product NDC | 51191-2015 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | titanium dioxide, octinoxate, octisalate, homosalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MULTALER & CIE S.A. |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 4; 7.5; 5; 11 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
