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SPF 20 UVA/UVB
SPF 20 UVA/UVB - 51191-2046-2 - (HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE)
Drug Information of SPF 20 UVA/UVB
| Product NDC: | 51191-2046 |
| Proprietary Name: | SPF 20 UVA/UVB |
| Non Proprietary Name: | HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 10; 7.5; 5; 2.7; 5 g/100g; g/100g; g/100g; g/100g; g/100g; g/100g & nbsp; HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SPF 20 UVA/UVB
| Product NDC: | 51191-2046 |
| Labeler Name: | MULTALER ET CIE S.A.S. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130415 |
Package Information of SPF 20 UVA/UVB
| Package NDC: | 51191-2046-2 |
| Package Description: | 150 g in 1 BOTTLE, SPRAY (51191-2046-2) |
NDC Information of SPF 20 UVA/UVB
| NDC Code | 51191-2046-2 |
| Proprietary Name | SPF 20 UVA/UVB |
| Package Description | 150 g in 1 BOTTLE, SPRAY (51191-2046-2) |
| Product NDC | 51191-2046 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130415 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | MULTALER ET CIE S.A.S. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 10; 7.5; 5; 2.7; 5 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
