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LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6
LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6 - 43455-0012-0 - (OCTINOXATE, OXYBENZONE)
Drug Information of LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6
| Product NDC: | 43455-0012 |
| Proprietary Name: | LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 2 g/100g; g/100g & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6
| Product NDC: | 43455-0012 |
| Labeler Name: | Ventura International, LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120324 |
Package Information of LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6
| Package NDC: | 43455-0012-0 |
| Package Description: | 8 g in 1 JAR (43455-0012-0) |
NDC Information of LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6
| NDC Code | 43455-0012-0 |
| Proprietary Name | LBEL EFFET PARFAIT Spots Reducing Effect Foundation SPF 18 - MEDIUM 6 |
| Package Description | 8 g in 1 JAR (43455-0012-0) |
| Product NDC | 43455-0012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120324 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ventura International, LTD |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 2 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
